A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6283416



Internal ID9655705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9395757..9397908hg38UCSC Ensembl
chr2:9535886..9538037hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg382152
hg192152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2662547
Supporting Variants
SamplesNA19385
Known GenesASAP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6283416
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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