A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5929011



Internal ID8906414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99956551..99962758hg38UCSC Ensembl
chr6:100404427..100410634hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg386208
hg196208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659885
Supporting Variants
SamplesNA19921
Known GenesMCHR2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5929011
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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