A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550745



Internal ID15991468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46289230hg38UCSC Ensembl
Innerchr10:47543322..47660466hg19UCSC Ensembl
Innerchr10:47013328..47130472hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38117145
hg19117145
hg18117145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1108n54
Supporting Variantsnssv747422
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550745
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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