A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097389



Internal ID21266899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:37709013..37719190hg38UCSC Ensembl
Innerchr5:37709115..37719292hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3810178
hg1910178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112295
Supporting Variants
Samplessample104
Known GenesWDR70
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097389
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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