A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029178



Internal ID21938521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41262627..41329403hg38UCSC Ensembl
chr17:39418879..39485655hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3866777
hg1966777
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636612
Samples
Known GenesKRTAP16-1, KRTAP17-1, KRTAP29-1, KRTAP9-6, KRTAP9-7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029178
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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