A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636226



Internal ID7023022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40447210..40451182hg38UCSC Ensembl
Innerchr15:40447360..40451032hg38UCSC Ensembl
Outerchr15:40447060..40451332hg38UCSC Ensembl
chr15:40739409..40743381hg19UCSC Ensembl
Innerchr15:40739559..40743231hg19UCSC Ensembl
Outerchr15:40739259..40743531hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg383973
hg193973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15227984, essv15227983
SamplesNA19404, NA19429
Known GenesBAHD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636226
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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