A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018547



Internal ID19107764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26265536..26424761hg38UCSC Ensembl
Innerchr9:26265534..26424759hg19UCSC Ensembl
Innerchr9:26255534..26414759hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38159226
hg19159226
hg18159226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7484n100
Supporting Variantsnssv3691988
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)nsv1018547
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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