A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6591283



Internal ID9562583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146716295..146716622hg38UCSC Ensembl
chr6:147037431..147037758hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2674520
Supporting Variants
SamplesNA19102
Known GenesADGB
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6591283
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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