A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669453



Internal ID15406105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:122922681..123005736hg38UCSC Ensembl
Innerchr2:123680257..123763312hg19UCSC Ensembl
Innerchr2:123396727..123479782hg18UCSC Ensembl
Innerchr2:123396487..123479542hg17UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3883056
hg1983056
hg1883056
hg1783056
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517668
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669453
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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