A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526883



Internal ID22396267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58074513..58074577hg38UCSC Ensembl
chr1:58540185..58540249hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv232n152
Supporting Variantsnssv14369606, nssv14369605
SamplesHG00512, HG00514
Known GenesDAB1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526883
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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