A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618144



Internal ID7005027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98054889..98064009hg38UCSC Ensembl
Innerchr8:98055389..98063509hg38UCSC Ensembl
Outerchr8:98053889..98065009hg38UCSC Ensembl
chr8:99067117..99076237hg19UCSC Ensembl
Innerchr8:99067617..99075737hg19UCSC Ensembl
Outerchr8:99066117..99077237hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg389121
hg199121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13267306, essv13267312, essv13267315, essv13267314, essv13267310, essv13267309, essv13267308, essv13267305, essv13267311, essv13267313, essv13267307
SamplesHG03121, NA19393, NA19107, NA19197, NA18520, NA19403, HG03397, HG03084, HG03351, NA19096, HG03470
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618144
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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