A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636244



Internal ID7023040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41428308..41434998hg38UCSC Ensembl
Innerchr15:41428358..41434948hg38UCSC Ensembl
Outerchr15:41428258..41435048hg38UCSC Ensembl
chr15:41720506..41727196hg19UCSC Ensembl
Innerchr15:41720556..41727146hg19UCSC Ensembl
Outerchr15:41720456..41727246hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg386691
hg196691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15230573
SamplesHG04210
Known GenesRTF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636244
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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