A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039203



Internal ID18781734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46295928hg38UCSC Ensembl
Innerchr10:47541177..47667164hg19UCSC Ensembl
Innerchr10:47011183..47137170hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38125988
hg19125988
hg18125988
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv833n100
Supporting Variantsnssv3514449, nssv3514631
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)nsv1039203
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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