A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664676



Internal ID9930781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113625059..113625931hg38UCSC Ensembl
chr13:114279374..114280246hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38873
hg19873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6586769, essv5924357, essv6091592, essv6105717, essv6337248, essv5709324, essv6395958, essv6517197
SamplesNA19397, NA20287, NA19404, HG01455, HG00731, NA19391, NA19395, NA19732
Known GenesTFDP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664676
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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