A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360399



Internal ID21017952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120823013..120823392hg38UCSC Ensembl
chr3:120541860..120542239hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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