A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025026



Internal ID21934369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33990757..33990915hg38UCSC Ensembl
chr11:34012304..34012462hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585787
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025026
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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