A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036968



Internal ID19126187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376297..20909084hg38UCSC Ensembl
Innerchr15:20581550..21114413hg19UCSC Ensembl
Innerchr15:18841564..19379038hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38532788
hg19532864
hg18537475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2245n100
Supporting Variantsnssv3714573
Samples
Known GenesCXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036968
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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