A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636983



Internal ID7023777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78473688..78475311hg38UCSC Ensembl
Innerchr15:78473738..78475261hg38UCSC Ensembl
Outerchr15:78473638..78475361hg38UCSC Ensembl
chr15:78766030..78767653hg19UCSC Ensembl
Innerchr15:78766080..78767603hg19UCSC Ensembl
Outerchr15:78765980..78767703hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381624
hg191624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15301376
SamplesHG02691
Known GenesIREB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636983
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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