A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045043



Internal ID19134262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25170021..25207565hg38UCSC Ensembl
Innerchr15:25415168..25452712hg19UCSC Ensembl
Innerchr15:22966261..23003805hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3837545
hg1937545
hg1837545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2480n100
Supporting Variantsnssv3545453
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, SNORD115-20, 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)nsv1045043
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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