A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608169



Internal ID6995099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15283782..15292099hg38UCSC Ensembl
Innerchr6:15283835..15292046hg38UCSC Ensembl
Outerchr6:15283729..15292152hg38UCSC Ensembl
chr6:15284013..15292330hg19UCSC Ensembl
Innerchr6:15284066..15292277hg19UCSC Ensembl
Outerchr6:15283960..15292383hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg388318
hg198318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12199836
SamplesHG02923
Known GenesJARID2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608169
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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