A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029000



Internal ID18771532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6188652..6687205hg38UCSC Ensembl
Innerchr9:6188652..6687205hg19UCSC Ensembl
Innerchr9:6178652..6677205hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38498554
hg19498554
hg18498554
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7386n100
Supporting Variantsnssv3692427
Samples
Known GenesGLDC, IL33, TPD52L3, UHRF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029000
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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