A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213769



Internal ID20780809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163995200..164055937hg38UCSC Ensembl
chr4:164916352..164977089hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3860738
hg1960738
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378817
Supporting Variants
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213769
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer