A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030719



Internal ID88186
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 StatusS
Merged Variantsnsv5555549
Supporting Variants
Samples
Known GenesCAMK1D, MIR4480
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030719
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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