A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616726



Internal ID6656922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27741299..27744731hg38UCSC Ensembl
Innerchr8:27741328..27744703hg38UCSC Ensembl
Outerchr8:27741271..27744760hg38UCSC Ensembl
chr8:27598816..27602248hg19UCSC Ensembl
Innerchr8:27598845..27602220hg19UCSC Ensembl
Outerchr8:27598788..27602277hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg383433
hg193433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13150589
SamplesHG04209
Known GenesCCDC25
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616726
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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