A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855977



Internal ID22630912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:70539794..70589630hg38UCSC Ensembl
chr13:71113926..71163762hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3849837
hg1949837
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455364, nssv17456405
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855977
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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