A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213764



Internal ID20780804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163727140..163743020hg38UCSC Ensembl
chr4:164648292..164664172hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3815881
hg1915881
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389152
Supporting Variants
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213764
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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