A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031673



Internal ID21941016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44567137..44568204hg38UCSC Ensembl
chr17:42644505..42645572hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381068
hg191068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031673
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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