A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527559



Internal ID22396946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149342155..149368521hg38UCSC Ensembl
chr7:149039246..149065612hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3826367
hg1926367
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338571, nssv14338570
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527559
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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