A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6075762



Internal ID9053165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29791414..29941747hg38UCSC Ensembl
chr6:29759191..29909524hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38150334
hg19150334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658390
Supporting Variants
SamplesNA20522
Known GenesHCG4, HCG4B, HLA-G, HLA-H, LOC554223
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6075762
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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