A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951550



Internal ID35058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88099868..88162636hg38UCSC Ensembl
chr4:89021020..89083788hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3862769
hg1962769
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464261
Supporting Variants
Samples
Known GenesABCG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951550
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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