A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917991



Internal ID22693212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27823846..27824161hg38UCSC Ensembl
chr10:28112775..28113090hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360484
Samples
Known GenesARMC4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917991
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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