A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570488



Internal ID21762531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22800693..22801000hg38UCSC Ensembl
chr7:22840312..22840619hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002074
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570488
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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