A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923668



Internal ID22698895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41102189..41154060hg38UCSC Ensembl
chr11:41123739..41175610hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3851872
hg1951872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369592
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923668
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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