A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609724



Internal ID20982795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:115832701..115861700hg38UCSC Ensembl
chr6:116153865..116182864hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3829000
hg1929000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609724
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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