A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545372



Internal ID18496967
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 StatusS
Merged Variantsnsv1045067
Supporting Variants
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)nssv3545372
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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