A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5662044



Internal ID8639447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29816860..30001630hg38UCSC Ensembl
chr6:29784637..29969407hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38184771
hg19184771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670487
Supporting Variants
SamplesNA18942
Known GenesHCG4B, HCG9, HLA-A, HLA-G, HLA-H, ZNRD1-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5662044
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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