A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930660



Internal ID22705930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10880831..10880960hg38UCSC Ensembl
chr19:10991507..10991636hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407052
Samples
Known GenesCARM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930660
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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