A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6499357



Internal ID9476760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138045057..138046064hg38UCSC Ensembl
chr4:138966211..138967218hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg381008
hg191008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667601
Supporting Variants
SamplesNA19455
Known GenesLINC00616
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6499357
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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