A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021917



Internal ID21931260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18268816..18268870hg38UCSC Ensembl
chr11:18290363..18290417hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578402
Samples
Known GenesSAA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021917
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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