A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097638



Internal ID21274810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36898721..36903980hg38UCSC Ensembl
Innerchr17:35255984..35261271hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg385260
hg195288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113974
Supporting Variants
Samplessample211
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097638
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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