A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229545



Internal ID20796585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:51391073..51393505hg38UCSC Ensembl
chr6:51255871..51258303hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg382433
hg192433
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396827
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229545
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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