A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944996



Internal ID22720468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82258565..82258767hg38UCSC Ensembl
chr13:82832700..82832902hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373191
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944996
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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