A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5793728



Internal ID9444556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195434925..195435318hg38UCSC Ensembl
chr3:195155654..195156047hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2662107
Supporting Variants
SamplesNA18858
Known GenesACAP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5793728
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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