A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618385



Internal ID7005267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:110028730..110035624hg38UCSC Ensembl
Innerchr8:110028730..110035624hg38UCSC Ensembl
Outerchr8:110028230..110036124hg38UCSC Ensembl
chr8:111040959..111047853hg19UCSC Ensembl
Innerchr8:111040959..111047853hg19UCSC Ensembl
Outerchr8:111040459..111048353hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg386895
hg196895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1410e214
Supporting Variantsessv13285664, essv13285665
SamplesHG01497, HG01269
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618385
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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