A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6247466



Internal ID9224869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115635740..115637772hg38UCSC Ensembl
chr3:115354587..115356619hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg382033
hg192033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672570
Supporting Variants
SamplesNA19398
Known GenesGAP43
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6247466
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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