A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051730



Internal ID19140949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30152061..30608663hg38UCSC Ensembl
Innerchr15:30444264..30900866hg19UCSC Ensembl
Innerchr15:28231556..28688158hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38456603
hg19456603
hg18456603
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2500n100
Supporting Variantsnssv3546508, nssv3546512, nssv3546514, nssv3721502, nssv3721504, nssv3546507, nssv3546510, nssv3721501, nssv3721503, nssv3546511, nssv3546513, nssv3546515, nssv3546509
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)nsv1051730
Frequency
Sample Size11257
Observed Gain4
Observed Loss9
Observed Complex0
Frequencyn/a


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