A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403708



Internal ID21061261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5039043..5891693hg38UCSC Ensembl
chr6:5039277..5891926hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38852651
hg19852650
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222216
Samples
Known GenesFARS2, LYRM4, MIR3691, PPP1R3G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403708
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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