A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944602



Internal ID22720069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:55173905..55177355hg38UCSC Ensembl
chr13:55748040..55751490hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg383451
hg193451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380289
Samples
Known GenesMIR5007
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944602
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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