A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046139



Internal ID19135358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25172299..25201209hg38UCSC Ensembl
Innerchr15:25417446..25446356hg19UCSC Ensembl
Innerchr15:22968539..22997449hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3828911
hg1928911
hg1828911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2480n100
Supporting Variantsnssv3545556, nssv3545557
Samples
Known GenesSNORD115-10, SNORD115-11, SNORD115-12, SNORD115-13, SNORD115-14, SNORD115-15, SNORD115-16, 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)nsv1046139
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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