A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563260



Internal ID21887615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90397502..90397682hg38UCSC Ensembl
chr7:90026816..90026996hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003316
Supporting Variants
Samples
Known GenesLOC101409256
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563260
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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