A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043107



Internal ID19132326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77156739..77171388hg38UCSC Ensembl
Innerchr9:79771655..79786304hg19UCSC Ensembl
Innerchr9:78961475..78976124hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3814650
hg1914650
hg1814650
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7683n100
Supporting Variantsnssv3696397
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)nsv1043107
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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