A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018801



Internal ID21928144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24141883..24149278hg38UCSC Ensembl
chr10:24430812..24438207hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg387396
hg197396
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586462
Samples
Known GenesKIAA1217
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018801
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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