A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355590



Internal ID21013143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114358593..114358964hg38UCSC Ensembl
chr3:114077440..114077811hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092747
Samples
Known GenesZBTB20, ZBTB20-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355590
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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