A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6274737



Internal ID9487600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50798243..50798554hg38UCSC Ensembl
chr6:50765956..50766267hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675117
Supporting Variants
SamplesNA18961
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6274737
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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