A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16889529



Internal ID167108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8946319..8952911hg38UCSC Ensembl
chr1:9006378..9012970hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg386593
hg196593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139069
Supporting Variants
Samples
Known GenesCA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16889529
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001718


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