A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001254



Internal ID21910597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63664773..63672747hg38UCSC Ensembl
chr10:65424533..65432507hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg387975
hg197975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579454
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001254
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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