A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947290



Internal ID22722793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31054662..31055188hg38UCSC Ensembl
chr13:31628799..31629325hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947290
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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