A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000444



Internal ID67875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97872394..97872456hg38UCSC Ensembl
chr7:97501706..97501768hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478995
Supporting Variants
Samples
Known GenesASNS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000444
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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