A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983622



Internal ID56461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35664023..35837660hg38UCSC Ensembl
chr6:35631800..35805437hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38173638
hg19173638
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473010
Supporting Variants
Samples
Known GenesARMC12, CLPS, CLPSL1, CLPSL2, FKBP5, LHFPL5, LOC285847, MIR5690, SRPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983622
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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