A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364554



Internal ID21022107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187118742..187141261hg38UCSC Ensembl
chr3:186836530..186859049hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3822520
hg1922520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099578
Samples
Known GenesRPL39L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364554
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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