A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890783



Internal ID19185085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:1244602..1277115hg38UCSC Ensembl
Outerchr6:1244602..1277115hg38UCSC Ensembl
Innerchr6:1244837..1277350hg19UCSC Ensembl
Outerchr6:1244837..1277350hg19UCSC Ensembl
Innerchr6:1189837..1222350hg18UCSC Ensembl
Outerchr6:1189837..1222350hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3832514
hg1932514
hg1832514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787032
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890783
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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