A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097641



Internal ID21274853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:48589299..48593927hg38UCSC Ensembl
Innerchr17:46666661..46671289hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg384629
hg194629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112840
Supporting Variants
Samplessample213
Known GenesHOXB5, HOXB-AS3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097641
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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