A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710800



Internal ID134466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1231302..1276710hg38UCSC Ensembl
chr17:1134596..1180004hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3845409
hg1945409
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557949
Supporting Variants
Samples
Known GenesBHLHA9
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710800
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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