A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047676



Internal ID19136895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25170021..25224900hg38UCSC Ensembl
Innerchr15:25415168..25470047hg19UCSC Ensembl
Innerchr15:22966261..23021140hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3854880
hg1954880
hg1854880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2482n100
Supporting Variantsnssv3545457, nssv3545456, nssv3545455
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, SNORD115-36, 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)nsv1047676
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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