A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940206



Internal ID22715612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37983710..37987488hg38UCSC Ensembl
chr13:38557847..38561625hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg383779
hg193779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386496
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940206
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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