A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982117



Internal ID55436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37117635..37118160hg38UCSC Ensembl
chr6:37085411..37085936hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140910
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982117
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001094


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