A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6261065



Internal ID9238468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165693497..165694036hg38UCSC Ensembl
chr4:166614649..166615188hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675884
Supporting Variants
SamplesNA18856
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6261065
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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