A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212039



Internal ID20779079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147826520..147845090hg38UCSC Ensembl
chr4:148747671..148766241hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3818571
hg1918571
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383434
Supporting Variants
Samples
Known GenesARHGAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212039
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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