A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800017



Internal ID19169625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:3973699..4000794hg38UCSC Ensembl
Innerchr12:4082865..4109960hg19UCSC Ensembl
Innerchr12:3953126..3980221hg18UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3827096
hg1927096
hg1827096
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892127
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800017
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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