A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6433070



Internal ID9161920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:127704247..127717677hg38UCSC Ensembl
Outerchr8:127704210..127717727hg38UCSC Ensembl
Innerchr8:128716492..128729923hg19UCSC Ensembl
Outerchr8:128716455..128729973hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3813518
hg1913519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658660
Supporting Variants
SamplesHG01357
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6433070
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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