A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv466862



Internal ID15180241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34695956..35011695hg38UCSC Ensembl
Innerchr10:34984884..35300623hg19UCSC Ensembl
Innerchr10:35024890..35340629hg18UCSC Ensembl
Innerchr10:35024890..35340629hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38315740
hg19315740
hg18315740
hg17315740
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv542316
SamplesHGDP00929
Known GenesCUL2, PARD3, PARD3-AS1
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)nsv466862
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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