A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv920279



Internal ID15867549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:143924451..143939546hg38UCSC Ensembl
Innerchr2:144682018..144697113hg19UCSC Ensembl
Innerchr2:144398488..144413583hg18UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg3815096
hg1915096
hg1815096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583247
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)nssv920279
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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