A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020663



Internal ID21930006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34655195..34656307hg38UCSC Ensembl
chr17:32982214..32983326hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381113
hg191113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636541
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020663
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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