A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667078



Internal ID9586497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29916720..30002248hg38UCSC Ensembl
chr6:29884497..29970025hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3885529
hg1985529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1088e199
Supporting Variantsessv5506776, essv5527009, essv6522095
SamplesHG00704, HG00656, NA19431
Known GenesHCG4B, HCG9, HLA-A, ZNRD1-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667078
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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