A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv465181



Internal ID15178560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143878890..144177097hg38UCSC Ensembl
Innerchr7:143575983..143874190hg19UCSC Ensembl
Innerchr7:143206916..143505123hg18UCSC Ensembl
Innerchr7:143013631..143311838hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38298208
hg19298208
hg18298208
hg17298208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv842n27
Supporting Variantsnssv541035
SamplesNINDS_149
Known GenesFAM115A, OR2A12, OR2A14, OR2A2, OR2A25, OR2A5, OR2F1, OR2F2, OR6B1
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)nsv465181
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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