A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6439745



Internal ID9479781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:194964203..194966108hg38UCSC Ensembl
chr2:195828927..195830832hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg381906
hg191906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664579
Supporting Variants
SamplesNA18950
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6439745
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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