A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606425



Internal ID20979496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158760231..158772974hg38UCSC Ensembl
chr6:159181263..159194006hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3812744
hg1912744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142005
Samples
Known GenesEZR, MIR3918, SYTL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606425
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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