A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6324678



Internal ID9740626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74817671..74827828hg38UCSC Ensembl
chr18:72529627..72539784hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3810158
hg1910158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657517
Supporting Variants
SamplesNA19676
Known GenesZNF407
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6324678
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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