A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698126



Internal ID15434778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:84514467..84558418hg38UCSC Ensembl
Innerchr9:87129382..87173333hg19UCSC Ensembl
Innerchr9:86319202..86363153hg18UCSC Ensembl
Innerchr9:84358936..84402887hg17UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3843952
hg1943952
hg1843952
hg1743952
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521509
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698126
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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