A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10632857



Internal ID4440317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:114729324..114751681hg38UCSC Ensembl
chr2:115486901..115509258hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3822358
hg1922358
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3592052
Supporting Variants
SamplesHG03949
Known GenesDPP10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10632857
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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