A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15316910



Internal ID5318726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88482984..88501253hg38UCSC Ensembl
Innerchr15:88483020..88501218hg38UCSC Ensembl
Outerchr15:88482949..88501289hg38UCSC Ensembl
chr15:89026215..89044484hg19UCSC Ensembl
Innerchr15:89026251..89044449hg19UCSC Ensembl
Outerchr15:89026180..89044520hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3818270
hg1918270
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637172
Supporting Variants
SamplesHG03074
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15316910
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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