A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109663



Internal ID20676703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1484712..1486437hg38UCSC Ensembl
chr4:1486437..1488162hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381726
hg191726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362484
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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