A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550778



Internal ID15991501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46224041..46295928hg38UCSC Ensembl
Innerchr10:47595277..47667164hg19UCSC Ensembl
Innerchr10:47065283..47137170hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3871888
hg1971888
hg1871888
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1116n54
Supporting Variantsnssv747549
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550778
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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