A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010708



Internal ID21920051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63094127..63096723hg38UCSC Ensembl
chr10:64853887..64856483hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382597
hg192597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584729
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010708
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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