A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275134



Internal ID348040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:35847544..35847585hg38UCSC Ensembl
Outerchr15:35847205..35849751hg38UCSC Ensembl
Innerchr15:36139745..36139786hg19UCSC Ensembl
Outerchr15:36139406..36141952hg19UCSC Ensembl
Innerchr15:33927037..33927078hg18UCSC Ensembl
Outerchr15:33926698..33929244hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg382547
hg192547
hg182547
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585480
Samples
Known GenesDPH6-AS1
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275134
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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