A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18113392



Internal ID20680432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25145456..25147058hg38UCSC Ensembl
chr4:25147078..25148680hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381603
hg191603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361426
Supporting Variants
Samples
Known GenesSEPSECS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18113392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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