A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3250178



Internal ID22377460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37506269..37506383hg38UCSC Ensembl
chr8:37363787..37363901hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14341213
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3250178
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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