A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995963



Internal ID64752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54671531..54712690hg38UCSC Ensembl
chr7:54739224..54780383hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3841160
hg1941160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474779
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995963
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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