A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909034



Internal ID22684244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97440959..97483202hg38UCSC Ensembl
chr10:99200716..99242959hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3842244
hg1942244
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357333
Samples
Known GenesEXOSC1, MMS19, ZDHHC16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909034
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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