A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5908306



Internal ID9330037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:40466455..40468680hg38UCSC Ensembl
Outerchr6:40466418..40468730hg38UCSC Ensembl
Innerchr6:40434194..40436419hg19UCSC Ensembl
Outerchr6:40434157..40436469hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg382313
hg192313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674055
Supporting Variants
SamplesNA18523
Known GenesLRFN2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5908306
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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