A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144638



Internal ID20711678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82262326..82266679hg38UCSC Ensembl
chr6:82972043..82976396hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg384354
hg194354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6397099
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144638
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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