A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987612



Internal ID59181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113947108..113947183hg38UCSC Ensembl
chr6:114268272..114268347hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459406
Supporting Variants
Samples
Known GenesHDAC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987612
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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