A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524116



Internal ID20897477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58041396..58045014hg38UCSC Ensembl
chr19:58552764..58556382hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg383619
hg193619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049028
Samples
Known GenesZSCAN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524116
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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