A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529557



Internal ID22398948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53349952..53350029hg38UCSC Ensembl
chr15:53642149..53642226hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14376992, nssv14382784
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529557
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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