A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3204566



Internal ID22353396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35628578..35628641hg38UCSC Ensembl
chr1:36094179..36094242hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14360645
SamplesHG00513
Known GenesPSMB2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3204566
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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