A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938170



Internal ID22713548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98476412..98478220hg38UCSC Ensembl
chr13:99128666..99130474hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381809
hg191809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372913
Samples
Known GenesSTK24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938170
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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