A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017622



Internal ID21926965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116831488..116831695hg38UCSC Ensembl
chr7:116471542..116471749hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576796
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017622
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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