A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036363



Internal ID19125582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100389827..100434244hg38UCSC Ensembl
Innerchr15:100930032..100974449hg19UCSC Ensembl
Innerchr15:98747555..98791972hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3844418
hg1944418
hg1844418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555328
Samples
Known GenesCERS3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036363
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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