A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000868



Internal ID21910211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12335606..12336177hg38UCSC Ensembl
chr10:12377605..12378176hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592014
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000868
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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