A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360577



Internal ID21018130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:19493869..19495590hg38UCSC Ensembl
chr3:19535361..19537082hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg381722
hg191722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101259
Samples
Known GenesKCNH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360577
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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