A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637005



Internal ID6677112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79730717..79746393hg38UCSC Ensembl
Innerchr15:79730754..79746356hg38UCSC Ensembl
Outerchr15:79730680..79746430hg38UCSC Ensembl
chr15:80023059..80038735hg19UCSC Ensembl
Innerchr15:80023096..80038698hg19UCSC Ensembl
Outerchr15:80023022..80038772hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3815677
hg1915677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15304731
SamplesHG02491
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637005
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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