A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6108464



Internal ID8739469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41897032..41897593hg38UCSC Ensembl
chr6:41864770..41865331hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660541
Supporting Variants
SamplesHG00125
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6108464
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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