A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359432



Internal ID21016985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134667393..134668034hg38UCSC Ensembl
chr3:134386235..134386876hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094839
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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