A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660736



Internal ID15397388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:120546972..120549106hg38UCSC Ensembl
Innerchr2:121304548..121306682hg19UCSC Ensembl
Innerchr2:121021018..121023152hg18UCSC Ensembl
Innerchr2:121020778..121022912hg17UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg382135
hg192135
hg182135
hg172135
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515554
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660736
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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