A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039641



Internal ID19128860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..20769398hg38UCSC Ensembl
Innerchr15:20564575..20974727hg19UCSC Ensembl
Innerchr15:18824589..19234772hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38410077
hg19410153
hg18410184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2228n100
Supporting Variantsnssv3537568, nssv3537567
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039641
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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