A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5590136



Internal ID9342323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13414860..13415570hg38UCSC Ensembl
Outerchr16:13414823..13415620hg38UCSC Ensembl
Innerchr16:13508717..13509427hg19UCSC Ensembl
Outerchr16:13508680..13509477hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664072
Supporting Variants
SamplesNA18539
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5590136
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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