A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525710



Internal ID22395088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41635541..41635625hg38UCSC Ensembl
chr1:42101212..42101296hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv194n152
Supporting Variantsnssv14363098, nssv14363102, nssv14363100, nssv14363103, nssv14363101, nssv14363096, nssv14363097, nssv14363099
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00513, HG00514
Known GenesHIVEP3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525710
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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