A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8808767



Internal ID13645321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75206184..75224377hg38UCSC Ensembl
Innerchr16:75208174..75222797hg38UCSC Ensembl
Outerchr16:75206074..75224497hg38UCSC Ensembl
chr16:75240082..75258275hg19UCSC Ensembl
Innerchr16:75242072..75256695hg19UCSC Ensembl
Outerchr16:75239972..75258395hg19UCSC Ensembl
chr16:73797583..73815776hg18UCSC Ensembl
Innerchr16:73799573..73814196hg18UCSC Ensembl
Outerchr16:73797473..73815896hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3818194
hg1918194
hg1818194
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3385328
Supporting Variants
SamplesNA12878
Known GenesCTRB1, CTRB2
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8808767
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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