A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6177886



Internal ID9155289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6224614..6227131hg38UCSC Ensembl
Outerchr16:6224457..6227284hg38UCSC Ensembl
Innerchr16:6274615..6277132hg19UCSC Ensembl
Outerchr16:6274458..6277285hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382828
hg192828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670124
Supporting Variants
SamplesHG00607
Known GenesRBFOX1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6177886
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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