A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660261



Internal ID9579680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133867536..134652360hg38UCSC Ensembl
Outerchr8:133867502..134652395hg38UCSC Ensembl
Innerchr8:134879779..135664603hg19UCSC Ensembl
Outerchr8:134879745..135664638hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38784894
hg19784894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6079207
SamplesHG00134
Known GenesZFAT, ZFAT-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660261
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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