A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708610



Internal ID132276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:72060682..72078386hg38UCSC Ensembl
chr16:72094581..72112285hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3817705
hg1917705
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432539
Supporting Variants
Samples
Known GenesHP, HPR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708610
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.051358


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