A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618099



Internal ID7004982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95400427..95410838hg38UCSC Ensembl
Innerchr8:95400427..95410838hg38UCSC Ensembl
Outerchr8:95400367..95410891hg38UCSC Ensembl
chr8:96412655..96423066hg19UCSC Ensembl
Innerchr8:96412655..96423066hg19UCSC Ensembl
Outerchr8:96412595..96423119hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3810412
hg1910412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13261586
SamplesHG02427
Known GenesLOC100616530
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618099
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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