A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044134



Internal ID19133353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77148171..77173657hg38UCSC Ensembl
Innerchr9:79763087..79788573hg19UCSC Ensembl
Innerchr9:78952907..78978393hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3825487
hg1925487
hg1825487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7681n100
Supporting Variantsnssv3696372
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)nsv1044134
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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