A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527006



Internal ID22396389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176430386..176430589hg38UCSC Ensembl
chr5:175857387..175857590hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14324683
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527006
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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