A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692402



Internal ID18990683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5065360..5081941hg38UCSC Ensembl
Innerchr9:5065360..5081941hg19UCSC Ensembl
Innerchr9:5055360..5071941hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3816582
hg1916582
hg1816582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017278
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)nssv3692402
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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