A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528202



Internal ID22397588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71928524..71928596hg38UCSC Ensembl
chr17:69924665..69924737hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3634n152
Supporting Variantsnssv14282586, nssv14282589, nssv14282587, nssv14282590, nssv14282588
SamplesHG00512, NA19238, NA19239, HG00731, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528202
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer