A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114988



Internal ID21298254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:29608608..29621375hg38UCSC Ensembl
Innerchr17:27935626..27948393hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3812768
hg1912768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098832
Samplessample116
Known GenesANKRD13B, CORO6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114988
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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