A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv456646



Internal ID15516711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24101079..24287455hg38UCSC Ensembl
Innerchr15:24346226..24532602hg19UCSC Ensembl
Innerchr15:21897319..22083695hg18UCSC Ensembl
Innerchr15:21897319..22083695hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38186377
hg19186377
hg18186377
hg17186377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv289n27
Supporting Variantsnssv533941
SamplesHGDP00313
Known GenesPWRN2
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)nsv456646
Frequency
Sample Size1557
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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