A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16999629



Internal ID67332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93615787..93616029hg38UCSC Ensembl
chr7:93245099..93245341hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483687
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16999629
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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