A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015095



Internal ID18757630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109683286..109700319hg38UCSC Ensembl
Innerchr1:110225908..110242941hg19UCSC Ensembl
Innerchr1:110027431..110044464hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3817034
hg1917034
hg1817034
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv269n100
Supporting Variantsnssv3485865, nssv3486791, nssv3490732, nssv3483969, nssv3494458, nssv3494759, nssv3500848, nssv3496088, nssv3496268, nssv3492445, nssv3486440, nssv3493330, nssv3485501, nssv3502569, nssv3499478, nssv3489714, nssv3701869, nssv3487124, nssv3496764, nssv3500904, nssv3497925, nssv3488153, nssv3498390, nssv3499886, nssv3498576, nssv3487422, nssv3498172, nssv3701870, nssv3502433, nssv3491746, nssv3488492, nssv3482957, nssv3491188, nssv3483556, nssv3490040, nssv3488961, nssv3500806, nssv3495341, nssv3483997, nssv3490387, nssv3701867, nssv3500564, nssv3498328, nssv3491406, nssv3501296, nssv3492156, nssv3493147, nssv3701866, nssv3490599, nssv3490464, nssv3502633, nssv3487866, nssv3486687, nssv3498483, nssv3493941, nssv3497789, nssv3487979, nssv3497885, nssv3497221, nssv3483394, nssv3486247, nssv3487862, nssv3500673, nssv3483782, nssv3489129, nssv3496027, nssv3488734, nssv3485546, nssv3502366, nssv3496528, nssv3492910, nssv3492590, nssv3485968, nssv3484189, nssv3490342, nssv3486735, nssv3701868, nssv3491849, nssv3488989, nssv3490099, nssv3488705, nssv3491530
Samples
Known GenesGSTM1, GSTM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015095
Frequency
Sample Size29084
Observed Gain37
Observed Loss45
Observed Complex0
Frequencyn/a


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