A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671175



Internal ID15407827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14216802..14231337hg38UCSC Ensembl
Innerchr2:14356926..14371461hg19UCSC Ensembl
Innerchr2:14274377..14288912hg18UCSC Ensembl
Innerchr2:14307524..14322059hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3814536
hg1914536
hg1814536
hg1714536
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517171
Supporting Variants
Samples
Known GenesLINC00276
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671175
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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