A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471630



Internal ID21129183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61626877..61627281hg38UCSC Ensembl
chr11:61394349..61394753hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993152
Samples
Known GenesRPLP0P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471630
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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