A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6229914



Internal ID9207317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162321869..162323900hg38UCSC Ensembl
chr2:163178379..163180410hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg382032
hg192032
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661102
Supporting Variants
SamplesNA19436
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6229914
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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