A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv466975



Internal ID15180354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46331279hg38UCSC Ensembl
Innerchr10:47543322..47702515hg19UCSC Ensembl
Innerchr10:47013328..47172521hg18UCSC Ensembl
Innerchr10:47013328..47172521hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38159194
hg19159194
hg18159194
hg17159194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv85n27
Supporting Variantsnssv542411
SamplesHGDP00888
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)nsv466975
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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