A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3715542



Internal ID19013823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22572335..22736951hg38UCSC Ensembl
Innerchr15:23136152..23300761hg19UCSC Ensembl
Innerchr15:20687593..20852202hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38164617
hg19164610
hg18164610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041383
Supporting Variants
Samples
Known GenesGOLGA8I, HERC2P2, WHAMMP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3715542
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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