A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051381



Internal ID18793912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8303425..8959142hg38UCSC Ensembl
Innerchr10:8345388..9001105hg19UCSC Ensembl
Innerchr10:8385394..9041111hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38655718
hg19655718
hg18655718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3501746
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)nsv1051381
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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