A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014378



Internal ID21923721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70918724..70918878hg38UCSC Ensembl
chr10:72678481..72678635hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014378
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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