A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545596



Internal ID18843877
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 StatusS
Merged Variantsnsv1044297
Supporting Variants
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)nssv3545596
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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