A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609128



Internal ID20982199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122413859..122415118hg38UCSC Ensembl
chr6:122735004..122736263hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg381260
hg191260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137372
Samples
Known GenesHSF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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