A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616539



Internal ID6656735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19191523..19245353hg38UCSC Ensembl
Innerchr8:19191541..19245335hg38UCSC Ensembl
Outerchr8:19191505..19245371hg38UCSC Ensembl
chr8:19049033..19102863hg19UCSC Ensembl
Innerchr8:19049051..19102845hg19UCSC Ensembl
Outerchr8:19049015..19102881hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3853831
hg1953831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1386e214
Supporting Variantsessv13131070
SamplesHG03871
Known GenesLOC100128993
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616539
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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