A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364577



Internal ID21022130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:29549380..29550915hg38UCSC Ensembl
chr3:29590871..29592406hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg381536
hg191536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102069
Samples
Known GenesRBMS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364577
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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