A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006939



Internal ID19096157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109684109..109697544hg38UCSC Ensembl
Innerchr1:110226731..110240166hg19UCSC Ensembl
Innerchr1:110028254..110041689hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3813436
hg1913436
hg1813436
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv267n100
Supporting Variantsnssv3701896, nssv3494026, nssv3701894, nssv3502203, nssv3485723, nssv3497197, nssv3499732, nssv3501263, nssv3499154, nssv3489653, nssv3491417, nssv3495270, nssv3486932, nssv3482981, nssv3495132, nssv3483013, nssv3486572, nssv3488635, nssv3492021, nssv3500578, nssv3492277, nssv3499690, nssv3701897, nssv3701895, nssv3487631, nssv3490379
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)nsv1006939
Frequency
Sample Size11257
Observed Gain1
Observed Loss25
Observed Complex0
Frequencyn/a


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