A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710884



Internal ID134550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2002441..2408835hg38UCSC Ensembl
chr17:1905735..2312129hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38406395
hg19406395
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554086
Supporting Variants
Samples
Known GenesDPH1, HIC1, LOC284009, MIR132, MIR212, MNT, OVCA2, RTN4RL1, SGSM2, SMG6, SNORD91A, SNORD91B, SRR, TSR1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710884
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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