A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033262



Internal ID19122484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12023071..12099446hg38UCSC Ensembl
Innerchr9:12023071..12099446hg19UCSC Ensembl
Innerchr9:12013071..12089446hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3876376
hg1976376
hg1876376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7445n100
Supporting Variantsnssv3690557
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)nsv1033262
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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