A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658199



Internal ID9924304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81121222..81123616hg38UCSC Ensembl
Outerchr16:81121065..81123769hg38UCSC Ensembl
Innerchr16:81154827..81157221hg19UCSC Ensembl
Outerchr16:81154670..81157374hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg382705
hg192705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv510e199
Supporting Variantsessv6459383
SamplesNA18561
Known GenesPKD1L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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