A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436432



Internal ID21093985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4908860..4909331hg38UCSC Ensembl
chr11:4930090..4930561hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38472
hg19472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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