A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6270778



Internal ID9415926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165828897..165830498hg38UCSC Ensembl
chr4:166750049..166751650hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656863
Supporting Variants
SamplesNA18617
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6270778
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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