A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5602506



Internal ID9685571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:144381974..144399183hg38UCSC Ensembl
chr3:144100816..144118025hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3817210
hg1917210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678593
Supporting Variants
SamplesNA19436
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5602506
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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