A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053435



Internal ID19142654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102832117..102971513hg38UCSC Ensembl
Innerchr9:105594399..105733795hg19UCSC Ensembl
Innerchr9:104634220..104773616hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38139397
hg19139397
hg18139397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7691n100
Supporting Variantsnssv3759798
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)nsv1053435
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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