A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053273



Internal ID18795804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25171567..25241470hg38UCSC Ensembl
Innerchr15:25416714..25486617hg19UCSC Ensembl
Innerchr15:22967807..23037710hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3869904
hg1969904
hg1869904
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2479n100
Supporting Variantsnssv3545519, nssv3545518, nssv3545517, nssv3545520
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, SNORD115-4, 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)nsv1053273
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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