A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608399



Internal ID6995329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26196282..26207207hg38UCSC Ensembl
chr6:26196510..26207435hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3810926
hg1910926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12232692, essv12232691, essv12232690, essv12232689
SamplesHG00244, HG02017, HG00451, HG01565
Known GenesHIST1H2AD, HIST1H2BF, HIST1H3D, HIST1H4E
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608399
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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