A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601522



Internal ID20974593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144180901..144188700hg38UCSC Ensembl
chr6:144502038..144509837hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216931
Samples
Known GenesSTX11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601522
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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