A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6461568



Internal ID9230863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69820428..69824902hg38UCSC Ensembl
chr16:69854331..69858805hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg384475
hg194475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671934
Supporting Variants
SamplesNA11918
Known GenesWWP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6461568
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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