A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363563



Internal ID21021116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149092060..149093664hg38UCSC Ensembl
chr3:148809847..148811451hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381605
hg191605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096292
Samples
Known GenesHLTF-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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