A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212124



Internal ID20779164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154586528..154603297hg38UCSC Ensembl
chr4:155507680..155524449hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3816770
hg1916770
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6388706
Supporting Variants
Samples
Known GenesFGA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212124
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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