A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981393



Internal ID54965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40098635..40134752hg38UCSC Ensembl
chr6:40066374..40102491hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3836118
hg1936118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464302
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981393
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002655


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