A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036662



Internal ID21946005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107367844..107372763hg38UCSC Ensembl
chr11:107238570..107243489hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg384920
hg194920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578474
Samples
Known GenesCWF19L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036662
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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