A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17001796



Internal ID68806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122130935..122131049hg38UCSC Ensembl
chr7:121770989..121771103hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486617
Supporting Variants
Samples
Known GenesAASS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17001796
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001561


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