A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008923



Internal ID18751454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240320793..240411537hg38UCSC Ensembl
Innerchr2:241260210..241350954hg19UCSC Ensembl
Innerchr2:240908883..240999627hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3890745
hg1990745
hg1890745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3729384
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008923
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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