A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555549



Internal ID328703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12255687..12698862hg38UCSC Ensembl
chr10:12297686..12740861hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38443176
hg19443176
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030719
Samples
Known GenesCAMK1D, MIR4480
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555549
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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