A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669174



Internal ID15405826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:139827494..139829172hg38UCSC Ensembl
Innerchr2:140585063..140586741hg19UCSC Ensembl
Innerchr2:140301533..140303211hg18UCSC Ensembl
Innerchr2:140418795..140420473hg17UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg381679
hg191679
hg181679
hg171679
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516560
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669174
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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