A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039207



Internal ID18781738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46176448..46278156hg38UCSC Ensembl
Innerchr10:47547684..47649392hg19UCSC Ensembl
Innerchr10:47017690..47119398hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38101709
hg19101709
hg18101709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv830n100
Supporting Variantsnssv3521265, nssv3510411
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039207
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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