A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545452



Internal ID18843733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25170021..25205630hg38UCSC Ensembl
Innerchr15:25415168..25450777hg19UCSC Ensembl
Innerchr15:22966261..23001870hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3835610
hg1935610
hg1835610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036680
Supporting Variants
Samples
Known GenesSNORD115-1, SNORD115-10, SNORD115-11, SNORD115-12, SNORD115-13, SNORD115-14, SNORD115-15, SNORD115-16, SNORD115-17, SNORD115-18, SNORD115-19, SNORD115-2, 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)nssv3545452
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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