A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212729



Internal ID20779769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156228574..156256205hg38UCSC Ensembl
chr4:157149726..157177357hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3827632
hg1927632
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393598
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212729
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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