A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107529



Internal ID20674570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103156426..103156947hg38UCSC Ensembl
chr4:104077583..104078104hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390382
Supporting Variants
Samples
Known GenesCENPE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107529
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00043


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