A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147441



Internal ID346622
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 StatusM
Merged Variants
Supporting Variantsnssv16955053
Samples
Known GenesAP1AR
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147441
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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