A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036680



Internal ID19125899
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 StatusM
Merged Variantsdgv2480n100
Supporting Variantsnssv3545452
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)nsv1036680
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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