A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784287



Internal ID19180494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103205897..103230167hg38UCSC Ensembl
Innerchr14:103672234..103696504hg19UCSC Ensembl
Innerchr14:102741987..102766257hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3824271
hg1924271
hg1824271
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892580
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784287
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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