A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5839390



Internal ID9118888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38364232..38378597hg38UCSC Ensembl
chr8:38221750..38236115hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3814366
hg1914366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675588
Supporting Variants
SamplesHG01133
Known GenesWHSC1L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5839390
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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