A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567638



Internal ID21759681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99609585..99609671hg38UCSC Ensembl
chr7:99207208..99207294hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012223
Supporting Variants
Samples
Known GenesLOC100289187
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567638
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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