A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6180456



Internal ID8946096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4733630..4736038hg38UCSC Ensembl
chr6:4733864..4736272hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg382409
hg192409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663092
Supporting Variants
SamplesHG00478
Known GenesCDYL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6180456
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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