A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525518



Internal ID22394896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:82356424..82356492hg38UCSC Ensembl
chr1:82822107..82822175hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14373884, nssv14376750
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525518
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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