A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051122



Internal ID18793653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77156739..77175939hg38UCSC Ensembl
Innerchr9:79771655..79790855hg19UCSC Ensembl
Innerchr9:78961475..78980675hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3819201
hg1919201
hg1819201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7682n100
Supporting Variantsnssv3697506
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)nsv1051122
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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