A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780521



Internal ID19178567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:27968331..28018965hg38UCSC Ensembl
Innerchr3:28009822..28060456hg19UCSC Ensembl
Innerchr3:27984826..28035460hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3850635
hg1950635
hg1850635
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893677
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780521
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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