A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv959824



Internal ID16253780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:16198127..16200987hg38UCSC Ensembl
Innerchr3:16239634..16242494hg19UCSC Ensembl
Innerchr3:16214638..16217498hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382861
hg192861
hg182861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589826
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)nssv959824
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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