A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939015



Internal ID22714403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27590734..27591018hg38UCSC Ensembl
chr13:28164871..28165155hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389206
Samples
Known GenesLNX2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939015
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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