A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2586044



Internal ID347623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:96771045..96773593hg38UCSC Ensembl
Outerchr15:96770048..96778448hg38UCSC Ensembl
Innerchr15:97314275..97316823hg19UCSC Ensembl
Outerchr15:97313278..97321678hg19UCSC Ensembl
Innerchr15:95115279..95117827hg18UCSC Ensembl
Outerchr15:95114282..95122682hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg388401
hg198401
hg188401
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275145
Supporting Variants
Samples
Known GenesSPATA8-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)essv2586044
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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