A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041356



Internal ID19130575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52376439..52440672hg38UCSC Ensembl
Innerchr10:54136199..54200432hg19UCSC Ensembl
Innerchr10:53806205..53870438hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3864234
hg1964234
hg1864234
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706907
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)nsv1041356
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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