A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030847



Internal ID19120066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22740233..22795972hg38UCSC Ensembl
Innerchr9:22740232..22795971hg19UCSC Ensembl
Innerchr9:22730232..22785971hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3855740
hg1955740
hg1855740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7476n100
Supporting Variantsnssv3690731
Samples
Known GenesFLJ35282
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030847
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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