A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3524970



Internal ID22394345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51580899..51580954hg38UCSC Ensembl
chr1:52046571..52046626hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv214n152
Supporting Variantsnssv14365927, nssv14365928
SamplesHG00512, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3524970
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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