A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032966



Internal ID19122188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7671812..7740619hg38UCSC Ensembl
Innerchr9:7671812..7740619hg19UCSC Ensembl
Innerchr9:7661812..7730619hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3868808
hg1968808
hg1868808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689107
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)nsv1032966
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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