A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6459405



Internal ID9569906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:149631480..149633433hg38UCSC Ensembl
Outerchr5:149631443..149633483hg38UCSC Ensembl
Innerchr5:149011043..149012996hg19UCSC Ensembl
Outerchr5:149011006..149013046hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382041
hg192041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671746
Supporting Variants
SamplesNA19129
Known GenesARHGEF37
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6459405
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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