A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv934846



Internal ID16228802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241915920..242093579hg38UCSC Ensembl
Innerchr2:242858071..243035730hg19UCSC Ensembl
Innerchr2:242506744..242684403hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38177660
hg19177660
hg18177660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585013
Supporting Variants
Samples
Known GenesLOC728323
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv934846
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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