A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6328917



Internal ID8807512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151421569..151422285hg38UCSC Ensembl
chr4:152342721..152343437hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2670825
Supporting Variants
SamplesHG00252
Known GenesFAM160A1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6328917
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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