A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047542



Internal ID18790073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32990472..33015005hg38UCSC Ensembl
Innerchr15:33282673..33307206hg19UCSC Ensembl
Innerchr15:31069965..31094498hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3824534
hg1924534
hg1824534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2549n100
Supporting Variantsnssv3547870
Samples
Known GenesFMN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047542
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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