A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6136536



Internal ID9723446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98392752..98405055hg38UCSC Ensembl
chr3:98111596..98123899hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3812304
hg1912304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677441
Supporting Variants
SamplesNA19474
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6136536
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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