A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045472



Internal ID18788003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46368035hg38UCSC Ensembl
Innerchr10:47541177..47739252hg19UCSC Ensembl
Innerchr10:47011183..47209258hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38198095
hg19198076
hg18198076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv837n100
Supporting Variantsnssv3514142
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045472
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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