A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892169



Internal ID19186565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:29790990..29821842hg38UCSC Ensembl
Outerchr12:29790990..29821842hg38UCSC Ensembl
Innerchr12:29943923..29974775hg19UCSC Ensembl
Outerchr12:29943923..29974775hg19UCSC Ensembl
Innerchr12:29835190..29866042hg18UCSC Ensembl
Outerchr12:29835190..29866042hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3830853
hg1930853
hg1830853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786928
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892169
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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