A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550767



Internal ID15991490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46184058..46332377hg38UCSC Ensembl
Innerchr10:47555294..47703613hg19UCSC Ensembl
Innerchr10:47025300..47173619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38148320
hg19148320
hg18148320
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1109n54
Supporting Variantsnssv747541, nssv747542, nssv747540
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550767
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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