A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5922571



Internal ID9723311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40334223..40351922hg38UCSC Ensembl
chr5:40334325..40352024hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3817700
hg1917700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661903
Supporting Variants
SamplesNA19474
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5922571
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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