A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001495



Internal ID21910838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117145948..117146087hg38UCSC Ensembl
chr10:118905459..118905598hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001495
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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