A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365913



Internal ID21023466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102714579..102715019hg38UCSC Ensembl
chr3:102433423..102433863hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090559
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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