A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674034



Internal ID9593453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16033794..16034203hg38UCSC Ensembl
Outerchr16:16033637..16034356hg38UCSC Ensembl
Innerchr16:16127651..16128060hg19UCSC Ensembl
Outerchr16:16127494..16128213hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5697211, essv6455503, essv5765088, essv5662544
SamplesNA18952, NA18945, NA18571, HG00671
Known GenesABCC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674034
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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