A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527599



Internal ID22396986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34265978..34266041hg38UCSC Ensembl
chr13:34840115..34840178hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14368092
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527599
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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