A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2763827



Internal ID17381495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46754541..46808658hg38UCSC Ensembl
Innerchr3:46796031..46850148hg19UCSC Ensembl
Innerchr3:46771035..46825152hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3854118
hg1954118
hg1854118
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv965407
Supporting Variants
SamplesHGDP00456
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2763827
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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