A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767754



Internal ID20543614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37215568..37215568hg38UCSC Ensembl
chr13:37789705..37789705hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294374
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767754
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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