A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6046668



Internal ID9024071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33160969..33161762hg38UCSC Ensembl
chr19:33651875..33652668hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677868
Supporting Variants
SamplesHG00473
Known GenesWDR88
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6046668
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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