A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048286



Internal ID19137505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:111156012..111241347hg38UCSC Ensembl
Innerchr10:112915770..113001105hg19UCSC Ensembl
Innerchr10:112905760..112991095hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3885336
hg1985336
hg1885336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510743
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)nsv1048286
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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