A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6268432



Internal ID9352766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37936926..37945436hg38UCSC Ensembl
chr3:37978417..37986927hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg388511
hg198511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676043
Supporting Variants
SamplesNA18548
Known GenesCTDSPL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6268432
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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