A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946803



Internal ID22722300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100735524..100735593hg38UCSC Ensembl
chr13:101387778..101387847hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369295
Samples
Known GenesNALCN-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946803
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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