A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662924



Internal ID9929029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:160307872..160310422hg38UCSC Ensembl
Outerchr2:160307715..160310575hg38UCSC Ensembl
Innerchr2:161164383..161166933hg19UCSC Ensembl
Outerchr2:161164226..161167086hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg382861
hg192861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv743e199
Supporting Variantsessv5672622
SamplesNA19701
Known GenesRBMS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662924
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