A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010598



Internal ID21919941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138244585..138270479hg38UCSC Ensembl
chr7:137929331..137955224hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3825895
hg1925894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572657
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010598
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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