A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037337



Internal ID19126556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25172299..25251453hg38UCSC Ensembl
Innerchr15:25417446..25496600hg19UCSC Ensembl
Innerchr15:22968539..23047693hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3879155
hg1979155
hg1879155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2485n100
Supporting Variantsnssv3545574, nssv3545573, nssv3545572
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, SNORD115-32, SNORD115-33, SNORD115-34, SNORD115-35, SNORD115-36, SNORD115-37, SNORD115-38, SNORD115-39, SNORD115-4, SNORD115-40, SNORD115-41, SNORD115-42, SNORD115-43, SNORD115-44, 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)nsv1037337
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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