A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918944



Internal ID22694166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24078788..24083887hg38UCSC Ensembl
chr10:24367717..24372816hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356183
Samples
Known GenesKIAA1217
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918944
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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