A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5527009



Internal ID8504412
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 Flag1
Merged StatusS
Merged Variantsesv2667078
Supporting Variants
SamplesNA19431
Known GenesHCG4B, HCG9, HLA-A, ZNRD1-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5527009
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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