A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034873



Internal ID19124093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23327227..23410598hg38UCSC Ensembl
Innerchr9:23327225..23410596hg19UCSC Ensembl
Innerchr9:23317225..23400596hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3883372
hg1983372
hg1883372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7477n100
Supporting Variantsnssv3690737
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)nsv1034873
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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