A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610945



Internal ID6997861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137710669..137726923hg38UCSC Ensembl
Innerchr6:137710819..137726773hg38UCSC Ensembl
Outerchr6:137710519..137727073hg38UCSC Ensembl
chr6:138031806..138048060hg19UCSC Ensembl
Innerchr6:138031956..138047910hg19UCSC Ensembl
Outerchr6:138031656..138048210hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3816255
hg1916255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1223e214
Supporting Variantsessv12565547, essv12565548
SamplesHG03490, HG00266
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610945
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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