A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11025933



Internal ID5010990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:60840853..60932975hg38UCSC Ensembl
chr3:60826517..60918647hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3892123
hg1992131
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596323
Supporting Variants
SamplesNA18507
Known GenesFHIT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11025933
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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