A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617182



Internal ID7004068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50693535..50779426hg38UCSC Ensembl
Innerchr8:50693535..50779426hg38UCSC Ensembl
Outerchr8:50693035..50779926hg38UCSC Ensembl
chr8:51606095..51691986hg19UCSC Ensembl
Innerchr8:51606095..51691986hg19UCSC Ensembl
Outerchr8:51605595..51692486hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3885892
hg1985892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13198102
SamplesNA18602
Known GenesSNTG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617182
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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