A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515643



Internal ID20889004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11126036..11126827hg38UCSC Ensembl
chr19:11236712..11237503hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38792
hg19792
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198056
Samples
Known GenesLDLR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515643
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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