A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469056



Internal ID15529121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:7847740..7970710hg38UCSC Ensembl
Innerchr12:8000336..8123306hg19UCSC Ensembl
Innerchr12:7891603..8014573hg18UCSC Ensembl
Innerchr12:7891603..8014573hg17UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38122971
hg19122971
hg18122971
hg17122971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv180n27
Supporting Variantsnssv544068
SamplesHGDP00694
Known GenesSLC2A14, SLC2A3
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)nsv469056
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer