A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv461898



Internal ID15521963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1009968..1097166hg38UCSC Ensembl
Innerchr5:1010083..1097281hg19UCSC Ensembl
Innerchr5:1063083..1150281hg18UCSC Ensembl
Innerchr5:1063083..1150281hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3887199
hg1987199
hg1887199
hg1787199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv686n27
Supporting Variantsnssv538224
SamplesHGDP00602
Known GenesMIR4635, NKD2, SLC12A7
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)nsv461898
Frequency
Sample Size1557
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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