A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6562103



Internal ID9547461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157421599..157423873hg38UCSC Ensembl
chr5:156848607..156850881hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg382275
hg192275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678778
Supporting Variants
SamplesNA19079
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6562103
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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