A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018823



Internal ID19108040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30420468..30563356hg38UCSC Ensembl
Innerchr9:30420466..30563354hg19UCSC Ensembl
Innerchr9:30410466..30553354hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38142889
hg19142889
hg18142889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7504n100
Supporting Variantsnssv3688826
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)nsv1018823
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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