A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995094



Internal ID64161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30506829..30507416hg38UCSC Ensembl
chr7:30546445..30547032hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484497
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995094
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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