A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413202



Internal ID21070755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5006556..5154562hg38UCSC Ensembl
chr6:5006790..5154796hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38148007
hg19148007
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217703
Samples
Known GenesLYRM4, MIR3691, PPP1R3G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413202
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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