A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545513



Internal ID18843794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25171567..25224900hg38UCSC Ensembl
Innerchr15:25416714..25470047hg19UCSC Ensembl
Innerchr15:22967807..23021140hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3853334
hg1953334
hg1853334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052672
Supporting Variants
Samples
Known GenesPWAR4, SNORD115-10, SNORD115-11, SNORD115-12, SNORD115-13, SNORD115-14, SNORD115-15, SNORD115-16, SNORD115-17, SNORD115-18, SNORD115-19, SNORD115-2, SNORD115-20, SNORD115-21, SNORD115-22, SNORD115-23, SNORD115-24, SNORD115-25, SNORD115-26, SNORD115-27, SNORD115-28, SNORD115-29, SNORD115-3, SNORD115-36, SNORD115-4, SNORD115-43, SNORD115-5, SNORD115-6, SNORD115-7, SNORD115-8, SNORD115-9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3545513
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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