A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15321023



Internal ID1319179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92779607..92783405hg38UCSC Ensembl
Innerchr15:92779617..92783396hg38UCSC Ensembl
Outerchr15:92779598..92783415hg38UCSC Ensembl
chr15:93322837..93326635hg19UCSC Ensembl
Innerchr15:93322847..93326626hg19UCSC Ensembl
Outerchr15:93322828..93326645hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383799
hg193799
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637269
Supporting Variants
SamplesHG01167
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15321023
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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