A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006978



Internal ID21916321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6413482..6413537hg38UCSC Ensembl
chr10:6455444..6455499hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006978
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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