A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585700



Internal ID21534248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87976218..87976393hg38UCSC Ensembl
chr13:88628473..88628648hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098840
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585700
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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