A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365847



Internal ID21023400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:19195301..19313600hg38UCSC Ensembl
chr3:19236793..19355092hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38118300
hg19118300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101234
Samples
Known GenesKCNH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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