A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843028



Internal ID22617963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34866094..34876925hg38UCSC Ensembl
chr5:34866199..34877030hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3810832
hg1910832
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496629
Samples
Known GenesTTC23L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843028
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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