A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047298



Internal ID19136517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:117229988..117245221hg38UCSC Ensembl
Innerchr9:119992267..120007500hg19UCSC Ensembl
Innerchr9:119032088..119047321hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3815234
hg1915234
hg1815234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695204
Samples
Known GenesASTN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047298
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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