A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6550713



Internal ID9528116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:246450..249976hg38UCSC Ensembl
chr16:296449..299975hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383527
hg193527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667528
Supporting Variants
SamplesNA19457
Known GenesITFG3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6550713
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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