A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636243



Internal ID7023039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41419786..41421669hg38UCSC Ensembl
Innerchr15:41419817..41421638hg38UCSC Ensembl
Outerchr15:41419755..41421700hg38UCSC Ensembl
chr15:41711984..41713867hg19UCSC Ensembl
Innerchr15:41712015..41713836hg19UCSC Ensembl
Outerchr15:41711953..41713898hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381884
hg191884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15230572
SamplesNA18990
Known GenesRTF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636243
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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