A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555218



Internal ID18506813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90453811..90841192hg38UCSC Ensembl
Innerchr15:90997043..91384422hg19UCSC Ensembl
Innerchr15:88798047..89185426hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38387382
hg19387380
hg18387380
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045042
Supporting Variants
Samples
Known GenesBLM, CRTC3, IQGAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3555218
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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