A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050817



Internal ID19140036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:119511961..119545569hg38UCSC Ensembl
Innerchr9:122274239..122307847hg19UCSC Ensembl
Innerchr9:121314060..121347668hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3833609
hg1933609
hg1833609
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695208
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)nsv1050817
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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