A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6376254



Internal ID9353657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:165517..184688hg38UCSC Ensembl
Outerchr16:165360..184841hg38UCSC Ensembl
Innerchr16:215516..234687hg19UCSC Ensembl
Outerchr16:215359..234840hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3819482
hg1919482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662940
Supporting Variants
SamplesHG00684
Known GenesHBA1, HBA2, HBM, HBQ1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6376254
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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