A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046814



Internal ID18789345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46264919..46333389hg38UCSC Ensembl
Innerchr10:47636155..47704625hg19UCSC Ensembl
Innerchr10:47106161..47174631hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3868471
hg1968471
hg1868471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv844n100
Supporting Variantsnssv3509272
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)nsv1046814
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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