A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035758



Internal ID19124977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65483607..65573102hg38UCSC Ensembl
Innerchr10:67243365..67332860hg19UCSC Ensembl
Innerchr10:66913371..67002866hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3889496
hg1989496
hg1889496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504105
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)nsv1035758
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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