A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636905



Internal ID7023699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74379726..74380483hg38UCSC Ensembl
Innerchr15:74379801..74380409hg38UCSC Ensembl
Outerchr15:74379652..74380558hg38UCSC Ensembl
chr15:74672067..74672824hg19UCSC Ensembl
Innerchr15:74672142..74672750hg19UCSC Ensembl
Outerchr15:74671993..74672899hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15292813
SamplesHG00338
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636905
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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