A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054676



Internal ID18797207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30201146..30608663hg38UCSC Ensembl
Innerchr15:30493349..30900866hg19UCSC Ensembl
Innerchr15:28280641..28688158hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38407518
hg19407518
hg18407518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2503n100
Supporting Variantsnssv3546615, nssv3546609, nssv3721533, nssv3546612, nssv3721532, nssv3546613, nssv3546614, nssv3546611, nssv3546608, nssv3546616, nssv3546610
Samples
Known GenesCHRFAM7A, DKFZP434L187, GOLGA8H, LOC101059918, ULK4P1, ULK4P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054676
Frequency
Sample Size29084
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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