A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16997311



Internal ID65752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43853868..43856383hg38UCSC Ensembl
chr7:43893467..43895982hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382516
hg192516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492104
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16997311
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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