A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6162794



Internal ID9140197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:138547617..138550730hg38UCSC Ensembl
Outerchr7:138547580..138550780hg38UCSC Ensembl
Innerchr7:138232362..138235475hg19UCSC Ensembl
Outerchr7:138232325..138235525hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg383201
hg193201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677536
Supporting Variants
SamplesHG00245
Known GenesTRIM24
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6162794
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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