A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035221



Internal ID18777752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43600874..43684208hg38UCSC Ensembl
Innerchr15:43893072..43976406hg19UCSC Ensembl
Innerchr15:41680364..41763698hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3883335
hg1983335
hg1883335
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2584n100
Supporting Variantsnssv3552284, nssv3716709, nssv3552293, nssv3552289, nssv3552296, nssv3716703, nssv3716706, nssv3552303, nssv3552287, nssv3552302, nssv3716705, nssv3716710, nssv3552299, nssv3552301, nssv3552292, nssv3716707, nssv3552283, nssv3552297, nssv3552305, nssv3552286, nssv3552288, nssv3552298, nssv3716704, nssv3552295, nssv3552285, nssv3552300, nssv3552291, nssv3716708, nssv3552294, nssv3552304, nssv3552290
Samples
Known GenesCATSPER2, RNU6-28P, STRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035221
Frequency
Sample Size29084
Observed Gain1
Observed Loss30
Observed Complex0
Frequencyn/a


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