A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940643



Internal ID22716054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87904006..87904364hg38UCSC Ensembl
chr13:88556261..88556619hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940643
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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