A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6540462



Internal ID9517866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:196611..198740hg38UCSC Ensembl
Outerchr16:196574..198790hg38UCSC Ensembl
Innerchr16:246610..248739hg19UCSC Ensembl
Outerchr16:246573..248789hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382217
hg192217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670048
Supporting Variants
SamplesNA19385
Known GenesLUC7L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6540462
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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