A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363837



Internal ID21021390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70294783..70295221hg38UCSC Ensembl
chr3:70343934..70344372hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103060
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363837
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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