A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550768



Internal ID15991491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46215343..46332710hg38UCSC Ensembl
Innerchr10:47586579..47703946hg19UCSC Ensembl
Innerchr10:47056585..47173952hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38117368
hg19117368
hg18117368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1113n54
Supporting Variantsnssv747543
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550768
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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