A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5458900



Internal ID9068471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:73875146..73875630hg38UCSC Ensembl
Outerchr2:73874989..73875783hg38UCSC Ensembl
Innerchr2:74102273..74102757hg19UCSC Ensembl
Outerchr2:74102116..74102910hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676949
Supporting Variants
SamplesHG00736
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5458900
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