A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212040



Internal ID20779080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147852364..148006326hg38UCSC Ensembl
chr4:148773515..148927477hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38153963
hg19153963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6382195
Supporting Variants
Samples
Known GenesARHGAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212040
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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