A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17001797



Internal ID68807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122139302..122146879hg38UCSC Ensembl
chr7:121779356..121786933hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg387578
hg197578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491546
Supporting Variants
Samples
Known GenesAASS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17001797
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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