A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429508



Internal ID21087061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54043925..54055677hg38UCSC Ensembl
chr8:54956485..54968237hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3811753
hg1911753
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230264
Samples
Known GenesLYPLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429508
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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