A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371506



Internal ID21029059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49549700..49558983hg38UCSC Ensembl
chr3:49587133..49596416hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg389284
hg199284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102675
Samples
Known GenesBSN, BSN-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371506
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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