A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890925



Internal ID19185321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103715663..104486604hg38UCSC Ensembl
Outerchr6:103715663..104486604hg38UCSC Ensembl
Innerchr6:104163538..104934479hg19UCSC Ensembl
Outerchr6:104163538..104934479hg19UCSC Ensembl
Innerchr6:104270231..105041172hg18UCSC Ensembl
Outerchr6:104270231..105041172hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38770942
hg19770942
hg18770942
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790994
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890925
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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