A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892656



Internal ID19183476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32159287..32341570hg38UCSC Ensembl
Outerchr15:32159287..32341570hg38UCSC Ensembl
Innerchr15:32451488..32633771hg19UCSC Ensembl
Outerchr15:32451488..32633771hg19UCSC Ensembl
Innerchr15:30238780..30421063hg18UCSC Ensembl
Outerchr15:30238780..30421063hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38182284
hg19182284
hg18182284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799427
Samples
Known GenesCHRNA7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892656
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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