A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985772



Internal ID57924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84212508..84213186hg38UCSC Ensembl
chr6:84922226..84922904hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467231
Supporting Variants
Samples
Known GenesKIAA1009
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985772
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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