A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576796



Internal ID21768839
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 StatusS
Merged Variantsnsv6017622
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576796
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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