A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636899



Internal ID6677006
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15292775, essv15292776
SamplesNA19780, HG01177
Known GenesPML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636899
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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