A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893578



Internal ID22668640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149420124..149507288hg38UCSC Ensembl
chr6:149741260..149828424hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3887165
hg1987165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424592
Samples
Known GenesPPIL4, ZC3H12D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893578
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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