A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6007922



Internal ID9159432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17135313..17140506hg38UCSC Ensembl
Outerchr8:17135276..17140556hg38UCSC Ensembl
Innerchr8:16992822..16998015hg19UCSC Ensembl
Outerchr8:16992785..16998065hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg385281
hg195281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663027
Supporting Variants
SamplesHG01354
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6007922
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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