A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970936



Internal ID47964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144406982..144419393hg38UCSC Ensembl
chr6:144728118..144740529hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3812412
hg1912412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464084
Supporting Variants
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970936
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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