A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035471



Internal ID21944814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63457002..63457130hg38UCSC Ensembl
chr17:61534363..61534491hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035471
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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