A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636248



Internal ID7023044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41777913..41778882hg38UCSC Ensembl
Innerchr15:41777963..41778832hg38UCSC Ensembl
Outerchr15:41777859..41778936hg38UCSC Ensembl
chr15:42070111..42071080hg19UCSC Ensembl
Innerchr15:42070161..42071030hg19UCSC Ensembl
Outerchr15:42070057..42071134hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38970
hg19970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15230578
SamplesNA18627
Known GenesMAPKBP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636248
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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