A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585009



Internal ID16372418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241915920..242080869hg38UCSC Ensembl
Innerchr2:242858071..243023020hg19UCSC Ensembl
Innerchr2:242506744..242671693hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38164950
hg19164950
hg18164950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7399n54
Supporting Variantsnssv934842
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585009
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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