A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023020



Internal ID21932363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2823913..2832324hg38UCSC Ensembl
chr17:2727207..2735618hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg388412
hg198412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635494
Samples
Known GenesRAP1GAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023020
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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