A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027866



Internal ID19117084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5065650..5083005hg38UCSC Ensembl
Innerchr9:5065650..5083005hg19UCSC Ensembl
Innerchr9:5055650..5073005hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3817356
hg1917356
hg1817356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7383n100
Supporting Variantsnssv3692404
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)nsv1027866
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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