A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034794



Internal ID19124015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12280677..12452015hg38UCSC Ensembl
Innerchr9:12280677..12452015hg19UCSC Ensembl
Innerchr9:12270677..12442015hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38171339
hg19171339
hg18171339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7454n100
Supporting Variantsnssv3690587
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)nsv1034794
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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