A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550747



Internal ID15991470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46295928hg38UCSC Ensembl
Innerchr10:47543322..47667164hg19UCSC Ensembl
Innerchr10:47013328..47137170hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38123843
hg19123843
hg18123843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1108n54
Supporting Variantsnssv1173600
SamplesHGDP00621
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550747
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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