A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545414



Internal ID18843695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25054112..25079530hg38UCSC Ensembl
Innerchr15:25299259..25324677hg19UCSC Ensembl
Innerchr15:22850352..22875770hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3825419
hg1925419
hg1825419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044940
Supporting Variants
Samples
Known GenesSNORD116-10, SNORD116-11, SNORD116-12, SNORD116-13, SNORD116-2, SNORD116-3, SNORD116-4, SNORD116-5, SNORD116-6, SNORD116-7, SNORD116-8, SNORD116-9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3545414
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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