A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004964



Internal ID70946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120876319..120946008hg38UCSC Ensembl
chr7:120516373..120586062hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3869690
hg1969690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475605
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004964
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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