A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223802



Internal ID20790842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63346927..63359567hg38UCSC Ensembl
chr6:64056832..64069472hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3812641
hg1912641
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412582
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223802
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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