A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv533932



Internal ID15156919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22788625..22997016hg38UCSC Ensembl
Innerchr15:22876052..23084443hg19UCSC Ensembl
Innerchr15:20427493..20635884hg18UCSC Ensembl
Innerchr15:20427493..20635884hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38208392
hg19208392
hg18208392
hg17208392
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv456636
Supporting Variants
Samples1780862356_A
Known GenesCYFIP1, NIPA1, NIPA2
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)nssv533932
Frequency
Sample Size1557
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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