A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211792



Internal ID20778832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25155720..25195541hg38UCSC Ensembl
chr4:25157342..25197163hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3839822
hg1939822
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356602
Supporting Variants
Samples
Known GenesSEPSECS, SEPSECS-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211792
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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