A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557461



Internal ID330558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:428013..744860hg38UCSC Ensembl
chr11:428013..744860hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38316848
hg19316848
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040936
Samples
Known GenesANO9, C11orf35, CDHR5, DEAF1, DRD4, EPS8L2, HRAS, IRF7, LOC143666, LRRC56, MIR210, MIR210HG, PHRF1, PTDSS2, RASSF7, RNH1, SCT, TMEM80
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557461
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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