A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6177896



Internal ID8944866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:63843769..63846216hg38UCSC Ensembl
Outerchr6:63843732..63846266hg38UCSC Ensembl
Innerchr6:64553662..64556109hg19UCSC Ensembl
Outerchr6:64553625..64556159hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg382535
hg192535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673667
Supporting Variants
SamplesHG00476
Known GenesEYS
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6177896
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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