A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040936



Internal ID95005
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 StatusS
Merged Variantsnsv5557461
Supporting Variants
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)nssv17040936
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.659226


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