A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471501



Internal ID21129054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118944725..118952080hg38UCSC Ensembl
chr11:118815434..118822790hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg387356
hg197357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986639
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471501
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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