A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616240



Internal ID7003127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11188121..11194751hg38UCSC Ensembl
Innerchr8:11188121..11194751hg38UCSC Ensembl
Outerchr8:11188061..11194794hg38UCSC Ensembl
chr8:11045630..11052260hg19UCSC Ensembl
Innerchr8:11045630..11052260hg19UCSC Ensembl
Outerchr8:11045570..11052303hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386631
hg196631
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13102314, essv13102315
SamplesHG04185, NA20906
Known GenesXKR6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616240
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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