A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658699



Internal ID9924804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37073235..37077555hg38UCSC Ensembl
chr6:37041011..37045331hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg384321
hg194321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6102024
SamplesHG00608
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658699
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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