A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890781



Internal ID19185083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:1188624..1247934hg38UCSC Ensembl
Outerchr6:1188624..1247934hg38UCSC Ensembl
Innerchr6:1188859..1248169hg19UCSC Ensembl
Outerchr6:1188859..1248169hg19UCSC Ensembl
Innerchr6:1133859..1193169hg18UCSC Ensembl
Outerchr6:1133859..1193169hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3859311
hg1959311
hg1859311
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790027
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890781
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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