A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003731



Internal ID21913074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119393117..119400355hg38UCSC Ensembl
chr6:119714282..119721520hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg387239
hg197239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565009
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003731
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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