A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999603



Internal ID19159140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:182600424..182686795hg38UCSC Ensembl
Innerchr2:183465151..183551522hg19UCSC Ensembl
Innerchr2:183173396..183259767hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3886372
hg1986372
hg1886372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3583127
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999603
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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