A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv468967



Internal ID15182346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:2118145..2158977hg38UCSC Ensembl
Innerchr12:2227311..2268143hg19UCSC Ensembl
Innerchr12:2097572..2138404hg18UCSC Ensembl
Innerchr12:2097572..2138404hg17UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3840833
hg1940833
hg1840833
hg1740833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv176n27
Supporting Variantsnssv543992
SamplesHGDP00708
Known GenesCACNA1C
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)nsv468967
Frequency
Sample Size1557
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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