A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218761



Internal ID20785801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37771878..37780662hg38UCSC Ensembl
chr6:37739654..37748438hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg388785
hg198785
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399759
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218761
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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