A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910197



Internal ID22685407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34061688..34061823hg38UCSC Ensembl
chr11:34083235..34083370hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361616
Samples
Known GenesCAPRIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910197
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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