A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677639



Internal ID15414291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21942429..21952245hg38UCSC Ensembl
Innerchr14:22410620..22420469hg19UCSC Ensembl
Innerchr14:21480460..21490309hg18UCSC Ensembl
Innerchr14:21480460..21490309hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg389817
hg199850
hg189850
hg179850
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520915
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677639
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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