A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6325681



Internal ID8750332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103173796..103201123hg38UCSC Ensembl
Outerchr6:103173639..103201276hg38UCSC Ensembl
Innerchr6:103621671..103648998hg19UCSC Ensembl
Outerchr6:103621514..103649151hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3827638
hg1927638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672112
Supporting Variants
SamplesHG00139
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6325681
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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