A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200407



Internal ID22349860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15904224..15904744hg38UCSC Ensembl
chr1:16230719..16231239hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14344051
SamplesNA19239
Known GenesSPEN
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200407
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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