A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039401



Internal ID19128620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25050690..25079530hg38UCSC Ensembl
Innerchr15:25295837..25324677hg19UCSC Ensembl
Innerchr15:22846930..22875770hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3828841
hg1928841
hg1828841
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2475n100
Supporting Variantsnssv3545399, nssv3545403, nssv3545402, nssv3545400, nssv3545401
Samples
Known GenesSNORD116-1, SNORD116-10, 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)nsv1039401
Frequency
Sample Size11257
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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