A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098974



Internal ID21272777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40817359..40820743hg38UCSC Ensembl
Innerchr17:38973611..38976995hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg383385
hg193385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114227
Supporting Variants
Samplessample182
Known GenesKRT10, TMEM99
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098974
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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