A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668024



Internal ID9934129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:42830482..42838858hg38UCSC Ensembl
Outerchr6:42830445..42838908hg38UCSC Ensembl
Innerchr6:42798220..42806596hg19UCSC Ensembl
Outerchr6:42798183..42806646hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg388464
hg198464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5958128
SamplesNA18548
Known GenesGLTSCR1L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668024
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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