A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200653



Internal ID22350070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52267933..52268035hg38UCSC Ensembl
chr4:53134099..53134201hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14312839
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200653
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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