A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5679405



Internal ID9683257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87767999..87774662hg38UCSC Ensembl
Outerchr4:87767962..87774712hg38UCSC Ensembl
Innerchr4:88689151..88695814hg19UCSC Ensembl
Outerchr4:88689114..88695864hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg386751
hg196751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678552
Supporting Variants
SamplesNA19435
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5679405
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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