A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904429



Internal ID16198385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:21674320..21729332hg38UCSC Ensembl
Innerchr2:21897192..21952204hg19UCSC Ensembl
Innerchr2:21750697..21805709hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3855013
hg1955013
hg1855013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581171
Supporting Variants
Samples
Known GenesLOC645949
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv904429
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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