A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044297



Internal ID19133516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25180179..25218319hg38UCSC Ensembl
Innerchr15:25425326..25463466hg19UCSC Ensembl
Innerchr15:22976419..23014559hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3838141
hg1938141
hg1838141
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2481n100
Supporting Variantsnssv3545596
Samples
Known GenesPWAR4, SNORD115-10, SNORD115-11, SNORD115-12, SNORD115-13, SNORD115-14, SNORD115-15, SNORD115-16, SNORD115-17, SNORD115-18, SNORD115-19, SNORD115-20, SNORD115-21, SNORD115-22, SNORD115-23, SNORD115-24, SNORD115-25, SNORD115-29, SNORD115-36, 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)nsv1044297
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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