A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6556569



Internal ID9533972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15977472..15983573hg38UCSC Ensembl
Outerchr16:15977435..15983623hg38UCSC Ensembl
Innerchr16:16071329..16077430hg19UCSC Ensembl
Outerchr16:16071292..16077480hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg386189
hg196189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661498
Supporting Variants
SamplesNA19099
Known GenesABCC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6556569
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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