A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051206



Internal ID18793737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132723216..132863839hg38UCSC Ensembl
Innerchr9:135598603..135739226hg19UCSC Ensembl
Innerchr9:134588424..134729047hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38140624
hg19140624
hg18140624
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696404, nssv3759839
Samples
Known GenesAK8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051206
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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