A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv466957



Internal ID15180336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46330334hg38UCSC Ensembl
Innerchr10:47543322..47701570hg19UCSC Ensembl
Innerchr10:47013328..47171576hg18UCSC Ensembl
Innerchr10:47013328..47171576hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38158249
hg19158249
hg18158249
hg17158249
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv85n27
Supporting Variantsnssv542393
SamplesHGDP00208
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisAn HMM examining LogR Ratio and B-allele Frequency was used to classify SNP array data into regions of copy-number 0-3. A combination of manual and automated curation was used on the resulting output to reduce false positives.
PlatformNot reported
Comments
ReferenceItsara_et_al_2009
Pubmed ID19166990
Accession Number(s)nsv466957
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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