A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355597



Internal ID21013150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49059080..49060206hg38UCSC Ensembl
chr3:49096513..49097639hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381127
hg191127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209348
Samples
Known GenesQRICH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355597
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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