A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6072119



Internal ID9750708
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 StatusS
Merged Variantsesv2676287
Supporting Variants
SamplesNA19701
Known GenesAGBL3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6072119
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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