A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610290



Internal ID6997207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107047051..107050834hg38UCSC Ensembl
Innerchr6:107047067..107050818hg38UCSC Ensembl
Outerchr6:107047035..107050850hg38UCSC Ensembl
chr6:107368255..107372038hg19UCSC Ensembl
Innerchr6:107368271..107372022hg19UCSC Ensembl
Outerchr6:107368239..107372054hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383784
hg193784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12499083, essv12499085, essv12499084
SamplesNA19072, NA19467, HG03103
Known GenesC6orf203
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610290
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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