A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005251



Internal ID71130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131973075..131982450hg38UCSC Ensembl
chr7:131657834..131667209hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg389376
hg199376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491491
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005251
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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