A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616714



Internal ID7003600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27148180..27157805hg38UCSC Ensembl
Innerchr8:27148180..27157805hg38UCSC Ensembl
Outerchr8:27148043..27157951hg38UCSC Ensembl
chr8:27005697..27015322hg19UCSC Ensembl
Innerchr8:27005697..27015322hg19UCSC Ensembl
Outerchr8:27005560..27015468hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg389626
hg199626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13150467
SamplesHG01883
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616714
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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