A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978096



Internal ID52802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6992712..6993282hg38UCSC Ensembl
chr6:6992945..6993515hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457349
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978096
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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