A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526872



Internal ID22396255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161151275..161151466hg38UCSC Ensembl
chr1:161121065..161121256hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14288735, nssv14288736, nssv14288734
SamplesHG00732, HG00733, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526872
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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