A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001919



Internal ID21911262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28361801..28362307hg38UCSC Ensembl
chr10:28650730..28651236hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38507
hg19507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001919
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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