A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6364268



Internal ID9232951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:45198711..45280074hg38UCSC Ensembl
Outerchr6:45198674..45280124hg38UCSC Ensembl
Innerchr6:45166448..45247811hg19UCSC Ensembl
Outerchr6:45166411..45247861hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3881451
hg1981451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668261
Supporting Variants
SamplesNA11920
Known GenesSUPT3H
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6364268
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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