A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560070



Internal ID22428866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91571765..91571765hg38UCSC Ensembl
chr13:92224019..92224019hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14370793
SamplesNA19240
Known GenesGPC5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560070
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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