A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6226094



Internal ID9203497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8732191..8733867hg38UCSC Ensembl
chr16:8826048..8827724hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381677
hg191677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660203
Supporting Variants
SamplesNA18520
Known GenesABAT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6226094
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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