A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030032



Internal ID21939375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95482725..95482781hg38UCSC Ensembl
chr11:95215889..95215945hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585433
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030032
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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