A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601173



Internal ID20974244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146508341..146554053hg38UCSC Ensembl
chr6:146829477..146875189hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3845713
hg1945713
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216958
Samples
Known GenesRAB32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601173
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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