A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050533



Internal ID19139752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105385380..105771818hg38UCSC Ensembl
Innerchr10:107145138..107531576hg19UCSC Ensembl
Innerchr10:107135128..107521566hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38386439
hg19386439
hg18386439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706218
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)nsv1050533
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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