A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6366731



Internal ID9035870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62168233..62171887hg38UCSC Ensembl
chr16:62202137..62205791hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg383655
hg193655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672547
Supporting Variants
SamplesHG00663
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6366731
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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