A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936254



Internal ID22711606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51416607..51417221hg38UCSC Ensembl
chr13:51990743..51991357hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387162
Samples
Known GenesINTS6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936254
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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