A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361466



Internal ID21019019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45547066..45554596hg38UCSC Ensembl
chr3:45588558..45596088hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg387531
hg197531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100658
Samples
Known GenesLARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361466
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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