A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372016



Internal ID21029569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70789678..70790124hg38UCSC Ensembl
chr3:70838829..70839275hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103727
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372016
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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