A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987716



Internal ID59254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118818126..118834853hg38UCSC Ensembl
chr6:119139289..119156016hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3816728
hg1916728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457610
Supporting Variants
Samples
Known GenesMCM9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987716
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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