A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786928



Internal ID19181834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:29790990..29821842hg38UCSC Ensembl
Innerchr12:29943923..29974775hg19UCSC Ensembl
Innerchr12:29835190..29866042hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3830853
hg1930853
hg1830853
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892169
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786928
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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