A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212138



Internal ID20779178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155818568..155830940hg38UCSC Ensembl
chr4:156739720..156752092hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3812373
hg1912373
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376882
Supporting Variants
Samples
Known GenesASIC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212138
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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