A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657486



Internal ID9923591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:34214143..34349157hg38UCSC Ensembl
chr4:34215765..34350779hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38135015
hg19135015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6321355
SamplesHG00629
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657486
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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