A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985015



Internal ID57399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87696470..87696747hg38UCSC Ensembl
chr6:88406188..88406465hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455862
Supporting Variants
Samples
Known GenesAKIRIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985015
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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