A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5499782



Internal ID9279241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158997850..158998678hg38UCSC Ensembl
chr6:159418882..159419710hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38829
hg19829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668232
Supporting Variants
SamplesNA12718
Known GenesRSPH3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5499782
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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