A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046793



Internal ID18789324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30201146..30483779hg38UCSC Ensembl
Innerchr15:30493349..30775982hg19UCSC Ensembl
Innerchr15:28280641..28563274hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38282634
hg19282634
hg18282634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2507n100
Supporting Variantsnssv3721516, nssv3546569
Samples
Known GenesCHRFAM7A, DKFZP434L187, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046793
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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