A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115523



Internal ID21298789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40817984..40820743hg38UCSC Ensembl
Innerchr17:38974236..38976995hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg382760
hg192760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097996
Samplessample33
Known GenesKRT10, TMEM99
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115523
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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