A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932899



Internal ID22708205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31077870..31078217hg38UCSC Ensembl
chr13:31652007..31652354hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932899
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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