A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700330



Internal ID15090296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106644208..106653011hg38UCSC Ensembl
Innerchr14:107100211..107109026hg19UCSC Ensembl
Innerchr14:106171256..106180071hg18UCSC Ensembl
Innerchr14:106171256..106180071hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg388804
hg198816
hg188816
hg178816
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517055
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700330
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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