A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029183



Internal ID19118402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30419932..30560431hg38UCSC Ensembl
Innerchr9:30419930..30560429hg19UCSC Ensembl
Innerchr9:30409930..30550429hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38140500
hg19140500
hg18140500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7504n100
Supporting Variantsnssv3755913, nssv3688808
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)nsv1029183
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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