A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350772



Internal ID22576441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41429032..41429796hg38UCSC Ensembl
chr11:41450582..41451346hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922116
Supporting Variants
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350772
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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