A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003012



Internal ID21912355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11885358..11885477hg38UCSC Ensembl
chr10:11927357..11927476hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596112
Samples
Known GenesPROSER2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003012
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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