A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800645



Internal ID19182398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:147722289..147789938hg38UCSC Ensembl
Innerchr6:148043425..148111074hg19UCSC Ensembl
Innerchr6:148085118..148152767hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3867650
hg1967650
hg1867650
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890962
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800645
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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