A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612099



Internal ID20985170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140364101..140384000hg38UCSC Ensembl
chr6:140685238..140705137hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3819900
hg1919900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216888
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612099
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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