A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593947



Internal ID21542539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34924128..34924306hg38UCSC Ensembl
chr13:35498265..35498443hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098207
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593947
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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