A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557885



Internal ID330965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9212349..9422366hg38UCSC Ensembl
chr3:9254033..9464050hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38210018
hg19210018
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930795
Samples
Known GenesSETD5, SETD5-AS1, SRGAP3, SRGAP3-AS3, THUMPD3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557885
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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