A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6349632



Internal ID8793416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143449800..143452648hg38UCSC Ensembl
chr8:144531970..144534818hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg382849
hg192849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673374
Supporting Variants
SamplesHG00237
Known GenesZC3H3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6349632
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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