A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045125



Internal ID18787656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19404194..19787121hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg18382928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2347n100
Supporting Variantsnssv3541438, nssv3541440, nssv3541439
Samples
Known GenesCT60, LOC727924
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045125
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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