A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6028909



Internal ID9006312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31388388..31485340hg38UCSC Ensembl
chr6:31356165..31453117hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3896953
hg1996953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674583
Supporting Variants
SamplesNA20276
Known GenesHCG26, HCP5, MICA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6028909
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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