A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054263



Internal ID19143482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102807930..102992459hg38UCSC Ensembl
Innerchr9:105570212..105754741hg19UCSC Ensembl
Innerchr9:104610033..104794562hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38184530
hg19184530
hg18184530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7691n100
Supporting Variantsnssv3697594
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)nsv1054263
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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