A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008146



Internal ID21917489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7499894..7500183hg38UCSC Ensembl
chr10:7541856..7542145hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596379
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008146
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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