A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985770



Internal ID57922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84139966..84139984hg38UCSC Ensembl
chr6:84849685..84849703hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5537286
Supporting Variants
Samples
Known GenesKIAA1009
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985770
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.160987


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