A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv934840



Internal ID16228796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241915920..242063126hg38UCSC Ensembl
Innerchr2:242858071..243005277hg19UCSC Ensembl
Innerchr2:242506744..242653950hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38147207
hg19147207
hg18147207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585007
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)nssv934840
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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