A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468572



Internal ID21126125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129724753..129727057hg38UCSC Ensembl
chr11:129594648..129596952hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382305
hg192305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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