A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050932



Internal ID19140151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24847119..24885605hg38UCSC Ensembl
Innerchr15:25092266..25130752hg19UCSC Ensembl
Innerchr15:22643359..22681845hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3838487
hg1938487
hg1838487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545396
Samples
Known GenesSNRPN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050932
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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