A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550794



Internal ID15991517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46259024..46281263hg38UCSC Ensembl
Innerchr10:47630260..47652499hg19UCSC Ensembl
Innerchr10:47100266..47122505hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3822240
hg1922240
hg1822240
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv747633, nssv747634
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550794
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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