A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692403



Internal ID18990684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5065360..5084696hg38UCSC Ensembl
Innerchr9:5065360..5084696hg19UCSC Ensembl
Innerchr9:5055360..5074696hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3819337
hg1919337
hg1819337
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029016
Supporting Variants
Samples
Known GenesJAK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3692403
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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