A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967956



Internal ID22742891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26242117..26242117hg38UCSC Ensembl
chr13:26816254..26816254hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379342
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967956
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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