A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970934



Internal ID47962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144370262..144375670hg38UCSC Ensembl
chr6:144691398..144696806hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg385409
hg195409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464883
Supporting Variants
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970934
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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