A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613176



Internal ID16053899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4921639..5003338hg38UCSC Ensembl
Innerchr9:4921639..5003338hg19UCSC Ensembl
Innerchr9:4911639..4993338hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3881700
hg1981700
hg1881700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126510
Samples
Known GenesJAK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613176
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer