A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044679



Internal ID19133898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52771774..52782251hg38UCSC Ensembl
Innerchr10:54531534..54542011hg19UCSC Ensembl
Innerchr10:54201540..54212017hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3810478
hg1910478
hg1810478
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516344
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)nsv1044679
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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