A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007780



Internal ID21917123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23024012..23024730hg38UCSC Ensembl
chr10:23312941..23313659hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38719
hg19719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586942
Samples
Known GenesARMC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007780
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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