A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6167952



Internal ID9657434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170343273..170344478hg38UCSC Ensembl
chr6:170652361..170653566hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381206
hg191206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2673814
Supporting Variants
SamplesNA19390
Known GenesFAM120B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6167952
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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