A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117128



Internal ID20684168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46489501..46491790hg38UCSC Ensembl
chr4:46491518..46493807hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg382290
hg192290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377805
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00052


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