A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011948



Internal ID21921291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16592118..16592184hg38UCSC Ensembl
chr10:16634117..16634183hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585868
Samples
Known GenesRSU1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011948
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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