A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692406



Internal ID18990687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5065766..5084214hg38UCSC Ensembl
Innerchr9:5065766..5084214hg19UCSC Ensembl
Innerchr9:5055766..5074214hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3818449
hg1918449
hg1818449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033735
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)nssv3692406
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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