A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986939



Internal ID58743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93096124..93100509hg38UCSC Ensembl
chr6:93805842..93810227hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg384386
hg194386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459552
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986939
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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