A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047227



Internal ID19136446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25172299..25198815hg38UCSC Ensembl
Innerchr15:25417446..25443962hg19UCSC Ensembl
Innerchr15:22968539..22995055hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3826517
hg1926517
hg1826517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2480n100
Supporting Variantsnssv3545555
Samples
Known GenesSNORD115-10, SNORD115-11, SNORD115-12, SNORD115-13, SNORD115-14, SNORD115-15, 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)nsv1047227
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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