A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530591



Internal ID20903952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36034492..36040555hg38UCSC Ensembl
chr19:36525394..36531457hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg386064
hg196064
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197799
Samples
Known GenesTHAP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530591
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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