A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463815



Internal ID21121368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68311901..68314600hg38UCSC Ensembl
chr11:68079369..68082068hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993568
Samples
Known GenesLRP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463815
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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