A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703795



Internal ID15440447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:88941919..88950908hg38UCSC Ensembl
Innerchr14:89408263..89417252hg19UCSC Ensembl
Innerchr14:88478016..88487005hg18UCSC Ensembl
Innerchr14:88478016..88487005hg17UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg388990
hg198990
hg188990
hg178990
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527364
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703795
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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