A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047745



Internal ID18790276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32567645hg38UCSC Ensembl
Innerchr15:32458661..32859846hg19UCSC Ensembl
Innerchr15:30245953..30647138hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38401186
hg19401186
hg18401186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2538n100
Supporting Variantsnssv3547755, nssv3547753, nssv3547754, nssv3547752, nssv3721619
Samples
Known GenesCHRNA7, GOLGA8K, GOLGA8O, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047745
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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