A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045067



Internal ID19134286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24792359..25083568hg38UCSC Ensembl
Innerchr15:25037506..25328715hg19UCSC Ensembl
Innerchr15:22588599..22879808hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38291210
hg19291210
hg18291210
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545372
Samples
Known GenesPWAR5, PWARSN, SNORD107, SNORD108, SNORD109A, SNORD109B, SNORD116-1, SNORD116-10, SNORD116-11, SNORD116-12, SNORD116-13, SNORD116-14, SNORD116-15, SNORD116-16, SNORD116-2, SNORD116-3, SNORD116-4, SNORD116-5, SNORD116-6, SNORD116-7, SNORD116-8, SNORD116-9, SNORD64, SNRPN, SNURF
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045067
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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