A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911158



Internal ID22686371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16560906..16566017hg38UCSC Ensembl
chr7:16600531..16605642hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg385112
hg195112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441283
Samples
Known GenesLRRC72
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911158
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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