A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700566



Internal ID15437218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83311559..83325861hg38UCSC Ensembl
Innerchr14:83777903..83792205hg19UCSC Ensembl
Innerchr14:82847656..82861958hg18UCSC Ensembl
Innerchr14:82847656..82861958hg17UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3814303
hg1914303
hg1814303
hg1714303
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524605
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700566
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer