A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705625



Internal ID129291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10000..34000hg38UCSC Ensembl
chr16:60001..84000hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3824001
hg1924000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146145
Supporting Variants
Samples
Known GenesDDX11L10, MIR6859-1, MIR6859-2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705625
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.029448


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