A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054373



Internal ID18796904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46203032..46333389hg38UCSC Ensembl
Innerchr10:47574268..47704625hg19UCSC Ensembl
Innerchr10:47044274..47174631hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38130358
hg19130358
hg18130358
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv835n100
Supporting Variantsnssv3520525, nssv3519645
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)nsv1054373
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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