A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464727



Internal ID21122280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37486962..37487582hg38UCSC Ensembl
chr11:37508512..37509132hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464727
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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