A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049863



Internal ID19139082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2379018..2500647hg38UCSC Ensembl
Innerchr10:2421212..2542839hg19UCSC Ensembl
Innerchr10:2411212..2532839hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38121630
hg19121628
hg18121628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv659n100
Supporting Variantsnssv3492263
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)nsv1049863
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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