A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948714



Internal ID21368783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96777996..96777996hg38UCSC Ensembl
chr15:97321226..97321226hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193839
SamplesHG002
Known GenesSPATA8-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948714
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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