A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv467182



Internal ID15180561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46238316..46324850hg38UCSC Ensembl
Innerchr10:47609552..47696086hg19UCSC Ensembl
Innerchr10:47079558..47166092hg18UCSC Ensembl
Innerchr10:47079558..47166092hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3886535
hg1986535
hg1886535
hg1786535
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv88n27
Supporting Variantsnssv542532
SamplesHGDP01018
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)nsv467182
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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