A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399759



Internal ID21057312
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 StatusM
Merged Variants
Supporting Variantsnssv18218761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399759
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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