A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6056647



Internal ID9615908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154359877..154362020hg38UCSC Ensembl
chr6:154681011..154683154hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg382144
hg192144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661081
Supporting Variants
SamplesNA19318
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6056647
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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