A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982819



Internal ID55902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54604931..54605285hg38UCSC Ensembl
chr6:54469729..54470083hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140533
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982819
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00266


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