A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031675



Internal ID19120897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5065360..5077985hg38UCSC Ensembl
Innerchr9:5065360..5077985hg19UCSC Ensembl
Innerchr9:5055360..5067985hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3812626
hg1912626
hg1812626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692398
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)nsv1031675
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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