A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670655



Internal ID15060621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:71100222..71115461hg38UCSC Ensembl
Innerchr2:71327352..71342591hg19UCSC Ensembl
Innerchr2:71180860..71196099hg18UCSC Ensembl
Innerchr2:71239007..71254246hg17UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3815240
hg1915240
hg1815240
hg1715240
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517762
Supporting Variants
Samples
Known GenesMCEE
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670655
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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