A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139459



Internal ID20706499
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 StatusS
Merged Variantsnsv6619420
Supporting Variants
Samples
Known GenesALDH8A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139459
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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