A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616162



Internal ID6656359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8987141..9062078hg38UCSC Ensembl
Innerchr8:8987141..9062078hg38UCSC Ensembl
Outerchr8:8986641..9062578hg38UCSC Ensembl
chr8:8844651..8919588hg19UCSC Ensembl
Innerchr8:8844651..8919588hg19UCSC Ensembl
Outerchr8:8844151..8920088hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3874938
hg1974938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13093754
SamplesNA20761
Known GenesERI1, MIR4660
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616162
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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