A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589353



Internal ID21781396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41305119..41305296hg38UCSC Ensembl
chr11:41326669..41326846hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031781
Supporting Variants
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589353
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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