A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15292775



Internal ID5294591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74013918..74018074hg38UCSC Ensembl
Innerchr15:74013918..74018074hg38UCSC Ensembl
Outerchr15:74013830..74018141hg38UCSC Ensembl
chr15:74306259..74310415hg19UCSC Ensembl
Innerchr15:74306259..74310415hg19UCSC Ensembl
Outerchr15:74306171..74310482hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg384157
hg194157
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636899
Supporting Variants
SamplesHG01177
Known GenesPML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15292775
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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