A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039180



Internal ID21948523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18982958..18983691hg38UCSC Ensembl
chr11:19004505..19005238hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039180
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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