A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987457



Internal ID59080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116410717..116410811hg38UCSC Ensembl
chr6:116731880..116731974hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471419
Supporting Variants
Samples
Known GenesDSE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987457
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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