A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036620



Internal ID21945963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42044994..42045060hg38UCSC Ensembl
chr17:40197012..40197078hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631451
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036620
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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