A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097645



Internal ID21274936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40817359..40821843hg38UCSC Ensembl
Innerchr17:38973611..38978095hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg384485
hg194485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110403
Supporting Variants
Samplessample214
Known GenesKRT10, TMEM99
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097645
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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