A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121815



Internal ID20688855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88204462..88210633hg38UCSC Ensembl
chr4:89125614..89131785hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg386172
hg196172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379421
Supporting Variants
Samples
Known GenesABCG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121815
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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