A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021761



Internal ID21931104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49057327..49060926hg38UCSC Ensembl
chr17:47134689..47138288hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632583
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021761
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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