A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049132



Internal ID18791663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:70280466..70390981hg38UCSC Ensembl
Innerchr9:72895382..73005897hg19UCSC Ensembl
Innerchr9:72085202..72195717hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38110516
hg19110516
hg18110516
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759766
Samples
Known GenesKLF9, SMC5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049132
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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