A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047920



Internal ID19137139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:84623328..84661280hg38UCSC Ensembl
Innerchr9:87238243..87276195hg19UCSC Ensembl
Innerchr9:86428063..86466015hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3837953
hg1937953
hg1837953
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697534
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047920
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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