A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6189674



Internal ID8907410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11747637..11749071hg38UCSC Ensembl
Outerchr16:11747600..11749121hg38UCSC Ensembl
Innerchr16:11841493..11842927hg19UCSC Ensembl
Outerchr16:11841456..11842977hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381522
hg191522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658473
Supporting Variants
SamplesHG00369
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6189674
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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