A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692245



Internal ID15428897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14216802..14239371hg38UCSC Ensembl
Innerchr2:14356926..14379495hg19UCSC Ensembl
Innerchr2:14274377..14296946hg18UCSC Ensembl
Innerchr2:14307524..14330093hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3822570
hg1922570
hg1822570
hg1722570
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)nssv692245
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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