A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636642



Internal ID7023436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59499548..59503800hg38UCSC Ensembl
Innerchr15:59499568..59503780hg38UCSC Ensembl
Outerchr15:59499528..59503820hg38UCSC Ensembl
chr15:59791747..59795999hg19UCSC Ensembl
Innerchr15:59791767..59795979hg19UCSC Ensembl
Outerchr15:59791727..59796019hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg384253
hg194253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15261099, essv15261100
SamplesNA19072, HG02760
Known GenesFAM81A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636642
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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