A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032703



Internal ID19121925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20264854..20287284hg38UCSC Ensembl
Innerchr9:20264852..20287282hg19UCSC Ensembl
Innerchr9:20254852..20277282hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3822431
hg1922431
hg1822431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7472n100
Supporting Variantsnssv3690698
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)nsv1032703
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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