A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563112



Internal ID336049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19578366..19611983hg38UCSC Ensembl
chr1:19904860..19938477hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3833618
hg1933618
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16902238
Samples
Known GenesMINOS1, MINOS1-NBL1, RPS14P3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563112
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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