A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695835



Internal ID15432487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47811079..47949956hg38UCSC Ensembl
Innerchr14:48280282..48419159hg19UCSC Ensembl
Innerchr14:47350032..47488909hg18UCSC Ensembl
Innerchr14:47350032..47488909hg17UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38138878
hg19138878
hg18138878
hg17138878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518404
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695835
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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