A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637012



Internal ID7023806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79924445..79953164hg38UCSC Ensembl
Innerchr15:79924945..79952664hg38UCSC Ensembl
Outerchr15:79923445..79954164hg38UCSC Ensembl
chr15:80216787..80245506hg19UCSC Ensembl
Innerchr15:80217287..80245006hg19UCSC Ensembl
Outerchr15:80215787..80246506hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3828720
hg1928720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15305124, essv15305123, essv15305125
SamplesNA18627, HG01800, HG01799
Known GenesC15orf37
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637012
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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