A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008891



Internal ID19098109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109684762..109697544hg38UCSC Ensembl
Innerchr1:110227384..110240166hg19UCSC Ensembl
Innerchr1:110028907..110041689hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3812783
hg1912783
hg1812783
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv267n100
Supporting Variantsnssv3491251, nssv3495256, nssv3483316, nssv3701955, nssv3488266, nssv3491075, nssv3497388, nssv3489817, nssv3701952, nssv3499247, nssv3702332, nssv3483699, nssv3496163, nssv3702330, nssv3492054, nssv3488459, nssv3486992, nssv3482827, nssv3502581, nssv3492673, nssv3491599, nssv3489418, nssv3492577, nssv3702329, nssv3499963, nssv3491067, nssv3701953, nssv3493692, nssv3485550, nssv3482942, nssv3492235, nssv3492742, nssv3489200, nssv3502424, nssv3484820, nssv3490902, nssv3702331, nssv3701956, nssv3500563, nssv3497628, nssv3495955, nssv3497448, nssv3487051, nssv3701954, nssv3495371, nssv3493096, nssv3484928, nssv3702327, nssv3490720, nssv3487687, nssv3487028, nssv3497396, nssv3493424, nssv3500890, nssv3495257, nssv3487384, nssv3487118, nssv3495120, nssv3497547, nssv3497841, nssv3501845, nssv3493083, nssv3486724, nssv3701951, nssv3484297, nssv3485540, nssv3498504, nssv3499747, nssv3495998, nssv3494365, nssv3496762, nssv3489291, nssv3501239, nssv3702328, nssv3491076, nssv3702326, nssv3491194, nssv3495924, nssv3494221, nssv3501738, nssv3499024, nssv3485592, nssv3701950, nssv3484343, nssv3483900, nssv3486573, nssv3490533, nssv3483666, nssv3494307, nssv3502688, nssv3483596
Samples
Known GenesGSTM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008891
Frequency
Sample Size11257
Observed Gain16
Observed Loss75
Observed Complex0
Frequencyn/a


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