A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550790



Internal ID15991513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46238316..46324850hg38UCSC Ensembl
Innerchr10:47609552..47696086hg19UCSC Ensembl
Innerchr10:47079558..47166092hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3886535
hg1986535
hg1886535
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1115n54
Supporting Variantsnssv1174533
SamplesHGDP01018
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550790
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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