A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660077



Internal ID15396729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:207491066..207493114hg38UCSC Ensembl
Innerchr2:208355790..208357838hg19UCSC Ensembl
Innerchr2:208064035..208066083hg18UCSC Ensembl
Innerchr2:208181296..208183344hg17UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg382049
hg192049
hg182049
hg172049
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515619
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660077
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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