A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6384599



Internal ID9608007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:4148566..4149211hg38UCSC Ensembl
chr5:4148679..4149324hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38646
hg19646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665123
Supporting Variants
SamplesNA19257
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6384599
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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