A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv909350



Internal ID16203306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52989779..53060928hg38UCSC Ensembl
Innerchr2:53216917..53288066hg19UCSC Ensembl
Innerchr2:53070421..53141570hg18UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3871150
hg1971150
hg1871150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581979
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv909350
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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