A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970509



Internal ID47667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143248189..143249149hg38UCSC Ensembl
chr6:143569326..143570286hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38961
hg19961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461510
Supporting Variants
Samples
Known GenesAIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970509
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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