A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229638



Internal ID20796678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43788183..43788349hg38UCSC Ensembl
chr6:43755920..43756086hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404921
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229638
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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