A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047075



Internal ID19136294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:80304115..80460034hg38UCSC Ensembl
Innerchr9:82919030..83074949hg19UCSC Ensembl
Innerchr9:82108850..82264769hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38155920
hg19155920
hg18155920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7685n100
Supporting Variantsnssv3697514
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)nsv1047075
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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