A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037848



Internal ID18780379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25170021..25239315hg38UCSC Ensembl
Innerchr15:25415168..25484462hg19UCSC Ensembl
Innerchr15:22966261..23035555hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3869295
hg1969295
hg1869295
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2479n100
Supporting Variantsnssv3545463, nssv3545465, nssv3545464
Samples
Known GenesPWAR4, SNORD115-1, 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, SNORD115-4, 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)nsv1037848
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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