A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv922090



Internal ID16216046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:155441262..155494920hg38UCSC Ensembl
Innerchr2:156297774..156351432hg19UCSC Ensembl
Innerchr2:156006020..156059678hg18UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3853659
hg1953659
hg1853659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583428
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)nssv922090
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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