A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209552



Internal ID20776592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112561701..112583900hg38UCSC Ensembl
chr4:113482857..113505056hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3822200
hg1922200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6382300
Supporting Variants
Samples
Known GenesC4orf21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209552
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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