A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv959847



Internal ID15907117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:16559591..16622096hg38UCSC Ensembl
Innerchr3:16601098..16663603hg19UCSC Ensembl
Innerchr3:16576102..16638607hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3862506
hg1962506
hg1862506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589839
Supporting Variants
Samples
Known GenesDAZL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv959847
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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