A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550792



Internal ID15991515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46239982..46295928hg38UCSC Ensembl
Innerchr10:47611218..47667164hg19UCSC Ensembl
Innerchr10:47081224..47137170hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3855947
hg1955947
hg1855947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1117n54
Supporting Variantsnssv1174535
SamplesHGDP01195
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550792
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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