A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550744



Internal ID15991467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46287904hg38UCSC Ensembl
Innerchr10:47543322..47659140hg19UCSC Ensembl
Innerchr10:47013328..47129146hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38115819
hg19115819
hg18115819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1108n54
Supporting Variantsnssv747420, nssv747421
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550744
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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