A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031427



Internal ID21940770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3003711..3005765hg38UCSC Ensembl
chr11:3024941..3026995hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382055
hg192055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587590
Samples
Known GenesCARS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031427
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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