A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6444865



Internal ID9607251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139284901..139286497hg38UCSC Ensembl
chr3:139003743..139005339hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381597
hg191597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658379
Supporting Variants
SamplesNA19257
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6444865
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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