A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037883



Internal ID19127102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25172299..25228106hg38UCSC Ensembl
Innerchr15:25417446..25473253hg19UCSC Ensembl
Innerchr15:22968539..23024346hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3855808
hg1955808
hg1855808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2485n100
Supporting Variantsnssv3545563
Samples
Known GenesPWAR4, 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, SNORD115-22, SNORD115-23, SNORD115-24, SNORD115-25, SNORD115-26, SNORD115-27, SNORD115-28, SNORD115-29, SNORD115-3, SNORD115-30, SNORD115-31, 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)nsv1037883
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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