A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569787



Internal ID16010510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65525552..65538180hg38UCSC Ensembl
Innerchr15:65817890..65830518hg19UCSC Ensembl
Innerchr15:63604943..63617571hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3812629
hg1912629
hg1812629
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844310
Samples
Known GenesPTPLAD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569787
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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