A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677002



Internal ID9596421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83651503..83658952hg38UCSC Ensembl
Outerchr16:83651466..83659002hg38UCSC Ensembl
Innerchr16:83685108..83692557hg19UCSC Ensembl
Outerchr16:83685071..83692607hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg387537
hg197537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5747945
SamplesNA19901
Known GenesCDH13
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677002
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer