A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457174



Internal ID21114727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96444063..96546590hg38UCSC Ensembl
chr11:96177227..96279755hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38102528
hg19102529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995464
Samples
Known GenesJRKL-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457174
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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