A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097673



Internal ID21275581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19866986..19868956hg38UCSC Ensembl
Innerchr17:19770299..19772269hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381971
hg191971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117652
Supporting Variants
Samplessample224
Known GenesULK2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097673
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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