A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212728



Internal ID20779768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156227520..156403891hg38UCSC Ensembl
chr4:157148672..157325043hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38176372
hg19176372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376236
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212728
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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