A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6498771



Internal ID9016450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:26776353..26778247hg38UCSC Ensembl
Outerchr16:26776196..26778400hg38UCSC Ensembl
Innerchr16:26787674..26789568hg19UCSC Ensembl
Outerchr16:26787517..26789721hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg382205
hg192205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676091
Supporting Variants
SamplesHG00629
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6498771
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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