A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037368



Internal ID21946711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62703409..62703482hg38UCSC Ensembl
chr11:62470881..62470954hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580216
Samples
Known GenesBSCL2, HNRNPUL2-BSCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037368
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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