A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979555



Internal ID53750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10352501..10356641hg38UCSC Ensembl
chr6:10352734..10356874hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg384141
hg194141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460486
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979555
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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