A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955053



Internal ID37347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112266428..112266560hg38UCSC Ensembl
chr4:113187584..113187716hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147441
Supporting Variants
Samples
Known GenesAP1AR
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955053
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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