A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636411



Internal ID6676518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48188917..48192173hg38UCSC Ensembl
Innerchr15:48188940..48192151hg38UCSC Ensembl
Outerchr15:48188895..48192196hg38UCSC Ensembl
chr15:48481114..48484370hg19UCSC Ensembl
Innerchr15:48481137..48484348hg19UCSC Ensembl
Outerchr15:48481092..48484393hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg383257
hg193257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15243867
SamplesHG04214
Known GenesCTXN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636411
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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