A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360771



Internal ID21018324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120537203..120537797hg38UCSC Ensembl
chr3:120256050..120256644hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360771
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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