A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714764



Internal ID19013045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381647..20609659hg38UCSC Ensembl
Innerchr15:20586900..20814965hg19UCSC Ensembl
Innerchr15:18846914..19074979hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38228013
hg19228066
hg18228066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039317
Supporting Variants
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3714764
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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