A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6250665



Internal ID9228068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10390570..10393829hg38UCSC Ensembl
chr16:10484427..10487686hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg383260
hg193260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2662100
Supporting Variants
SamplesNA19332
Known GenesATF7IP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6250665
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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