A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765780



Internal ID20541640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35022685..35022685hg38UCSC Ensembl
chr19:35513589..35513589hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289590
Samples
Known GenesGRAMD1A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765780
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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