A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv462428



Internal ID15175807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:88791695..88894106hg38UCSC Ensembl
Innerchr1:89257378..89359789hg19UCSC Ensembl
Innerchr1:89029966..89132377hg18UCSC Ensembl
Innerchr1:88969399..89071810hg17UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38102412
hg19102412
hg18102412
hg17102412
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv22n27
Supporting Variantsnssv538595
SamplesHGDP00995
Known GenesGTF2B, PKN2
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)nsv462428
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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