A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890962



Internal ID19185358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:147722289..147789938hg38UCSC Ensembl
Outerchr6:147722289..147789938hg38UCSC Ensembl
Innerchr6:148043425..148111074hg19UCSC Ensembl
Outerchr6:148043425..148111074hg19UCSC Ensembl
Innerchr6:148085118..148152767hg18UCSC Ensembl
Outerchr6:148085118..148152767hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3867650
hg1967650
hg1867650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800645
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890962
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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