A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6118580



Internal ID8975426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40310163..40311537hg38UCSC Ensembl
chr4:40312180..40313554hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381375
hg191375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658466
Supporting Variants
SamplesHG00556
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6118580
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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