A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970503



Internal ID47663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143195577..143195837hg38UCSC Ensembl
chr6:143516714..143516974hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464404
Supporting Variants
Samples
Known GenesAIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970503
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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