A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005365



Internal ID71197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155264461..155288948hg38UCSC Ensembl
chr7:155056171..155080658hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3824488
hg1924488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483132
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005365
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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