A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703354



Internal ID15440006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:86799185..86876637hg38UCSC Ensembl
Innerchr14:87265529..87342981hg19UCSC Ensembl
Innerchr14:86335282..86412734hg18UCSC Ensembl
Innerchr14:86335282..86412734hg17UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3877453
hg1977453
hg1877453
hg1777453
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526981
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703354
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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