A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv959822



Internal ID16253778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:16198127..16200402hg38UCSC Ensembl
Innerchr3:16239634..16241909hg19UCSC Ensembl
Innerchr3:16214638..16216913hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382276
hg192276
hg182276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589824
Supporting Variants
Samples
Known GenesGALNT15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv959822
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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