A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659082



Internal ID9925187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:101583518..101585509hg38UCSC Ensembl
Outerchr6:101583361..101585662hg38UCSC Ensembl
Innerchr6:102031393..102033384hg19UCSC Ensembl
Outerchr6:102031236..102033537hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg382302
hg192302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6229952
SamplesHG00427
Known GenesGRIK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659082
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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