A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545506



Internal ID18843787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25171567..25207907hg38UCSC Ensembl
Innerchr15:25416714..25453054hg19UCSC Ensembl
Innerchr15:22967807..23004147hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3836341
hg1936341
hg1836341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037152
Supporting Variants
Samples
Known GenesSNORD115-10, SNORD115-11, SNORD115-12, SNORD115-13, SNORD115-14, SNORD115-15, SNORD115-16, SNORD115-17, SNORD115-18, SNORD115-19, SNORD115-2, SNORD115-20, SNORD115-21, SNORD115-29, 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)nssv3545506
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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