A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437642



Internal ID21095195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19060612..19063306hg38UCSC Ensembl
chr11:19082159..19084853hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382695
hg192695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988696
Samples
Known GenesMRGPRX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437642
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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