A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619420



Internal ID20992491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134925701..134934400hg38UCSC Ensembl
chr6:135246839..135255538hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139459
Samples
Known GenesALDH8A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619420
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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