A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046522



Internal ID18789053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17345945..17375810hg38UCSC Ensembl
Innerchr10:17387944..17417809hg19UCSC Ensembl
Innerchr10:17427950..17457815hg18UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3829866
hg1929866
hg1829866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513041
Samples
Known GenesST8SIA6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046522
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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