A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6327638



Internal ID8928508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8432262..8434992hg38UCSC Ensembl
chr6:8432495..8435225hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg382731
hg192731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656617
Supporting Variants
SamplesHG00437
Known GenesSLC35B3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6327638
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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