A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526544



Internal ID22395924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:172492390..172492491hg38UCSC Ensembl
chr1:172461530..172461631hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14296605, nssv14296606, nssv14296604
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526544
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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