A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036250



Internal ID18778781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32147032..32565269hg38UCSC Ensembl
Innerchr15:32439233..32857470hg19UCSC Ensembl
Innerchr15:30226525..30644762hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38418238
hg19418238
hg18418238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2538n100
Supporting Variantsnssv3721606
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)nsv1036250
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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