A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963545



Internal ID16257501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61430495..61439491hg38UCSC Ensembl
Innerchr3:61416169..61425165hg19UCSC Ensembl
Innerchr3:61391209..61400205hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg388997
hg198997
hg188997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590432
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963545
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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