A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033417



Internal ID18775951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3594189..3732530hg38UCSC Ensembl
Innerchr9:3594189..3732530hg19UCSC Ensembl
Innerchr9:3584189..3722530hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38138342
hg19138342
hg18138342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7378n100
Supporting Variantsnssv3692370
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)nsv1033417
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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