A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023801



Internal ID21933144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62009599..62010378hg38UCSC Ensembl
chr11:61777071..61777850hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38780
hg19780
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595230
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023801
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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