A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527483



Internal ID22396869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155208171..155209003hg38UCSC Ensembl
chr7:154999881..155000713hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338120
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527483
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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