A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054462



Internal ID18796993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46331987hg38UCSC Ensembl
Innerchr10:47541177..47703223hg19UCSC Ensembl
Innerchr10:47011183..47173229hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38162047
hg19162047
hg18162047
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv836n100
Supporting Variantsnssv3508416, nssv3517913, nssv3706024
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)nsv1054462
Frequency
Sample Size29084
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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