A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396242



Internal ID21053795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52810953..52886773hg38UCSC Ensembl
chr6:52675751..52751571hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3875821
hg1975821
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223913
Samples
Known GenesGSTA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396242
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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