A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619753



Internal ID20992824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135668635..135676902hg38UCSC Ensembl
chr6:135989773..135998040hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg388268
hg198268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216020
Samples
Known GenesLINC00271
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619753
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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