A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783332



Internal ID19169198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78025956..78063157hg38UCSC Ensembl
Innerchr6:78735673..78772874hg19UCSC Ensembl
Innerchr6:78792392..78829593hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3837202
hg1937202
hg1837202
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890887
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783332
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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