A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404394



Internal ID21061947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87469001..87476100hg38UCSC Ensembl
chr6:88178719..88185818hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg387100
hg197100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236193
Samples
Known GenesSLC35A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404394
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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