A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563779



Internal ID336708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159807892..159974165hg38UCSC Ensembl
chr1:159777682..159943955hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38166274
hg19166274
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16891325
Samples
Known GenesC1orf204, CCDC19, FCRL6, IGSF9, LINC01133, SLAMF8, SLAMF9, TAGLN2, VSIG8
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563779
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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