A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028253



Internal ID19117471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11978901..12379463hg38UCSC Ensembl
Innerchr9:11978901..12379463hg19UCSC Ensembl
Innerchr9:11968901..12369463hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38400563
hg19400563
hg18400563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7426n100
Supporting Variantsnssv3690523
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)nsv1028253
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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