A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5757893



Internal ID8735296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29883589..29937895hg38UCSC Ensembl
Outerchr6:29883218..29938415hg38UCSC Ensembl
Innerchr6:29851366..29905672hg19UCSC Ensembl
Outerchr6:29850995..29906192hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3855198
hg1955198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674693
Supporting Variants
SamplesHG01353
Known GenesHCG4B, HLA-H
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5757893
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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