A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676287



Internal ID9942392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135013719..135014314hg38UCSC Ensembl
Outerchr7:135013562..135014467hg38UCSC Ensembl
Innerchr7:134698470..134699065hg19UCSC Ensembl
Outerchr7:134698313..134699218hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38906
hg19906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6072119, essv5736624, essv6342556
SamplesNA19701, NA19466, NA18858
Known GenesAGBL3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676287
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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