A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657841



Internal ID9577260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:84212596..84213137hg38UCSC Ensembl
Outerchr6:84212439..84213290hg38UCSC Ensembl
Innerchr6:84922314..84922855hg19UCSC Ensembl
Outerchr6:84922157..84923008hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38852
hg19852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6485279, essv6169399
SamplesHG00346, HG00329
Known GenesKIAA1009
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657841
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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