A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751704



Internal ID20527564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10879107..10879107hg38UCSC Ensembl
chr19:10989783..10989783hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291037
Samples
Known GenesCARM1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751704
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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