A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935618



Internal ID22710962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30612160..30612227hg38UCSC Ensembl
chr13:31186297..31186364hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386188
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935618
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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