A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033735



Internal ID19122956
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 StatusM
Merged Variantsdgv7383n100
Supporting Variantsnssv3692406
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)nsv1033735
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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