A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036561



Internal ID21945904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57797767..57797829hg38UCSC Ensembl
chr17:55875128..55875190hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622416
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036561
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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