A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937231



Internal ID21357301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73067663..73067663hg38UCSC Ensembl
chr8:73979898..73979898hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204095
SamplesHG002
Known GenesSBSPON
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937231
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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