A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867413



Internal ID22642348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:56527905..56530044hg38UCSC Ensembl
chr13:57102039..57104178hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg382140
hg192140
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467460, nssv17467584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867413
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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