A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038399



Internal ID19127618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77062503..77096821hg38UCSC Ensembl
Innerchr9:79677419..79711737hg19UCSC Ensembl
Innerchr9:78867239..78901557hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3834319
hg1934319
hg1834319
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759771
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)nsv1038399
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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