A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5788663



Internal ID9624451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48332683..48334345hg38UCSC Ensembl
chr4:48334700..48336362hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg381663
hg191663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660176
Supporting Variants
SamplesNA19334
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5788663
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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