A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359083



Internal ID21016636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49295018..49296378hg38UCSC Ensembl
chr3:49332451..49333811hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381361
hg191361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102037
Samples
Known GenesUSP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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