A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786095



Internal ID19180034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:113046486..113117593hg38UCSC Ensembl
Innerchr6:113367688..113438795hg19UCSC Ensembl
Innerchr6:113474381..113545488hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3871108
hg1971108
hg1871108
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890929
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786095
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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