A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526567



Internal ID22395948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:88993893..88993957hg38UCSC Ensembl
chr1:89459576..89459640hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14377096, nssv14391405, nssv14376119
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526567
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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