A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606715



Internal ID20979786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112502101..112535700hg38UCSC Ensembl
chr6:112823303..112856902hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3833600
hg1933600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216828
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606715
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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