A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782221



Internal ID19180890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:58828978..59154349hg38UCSC Ensembl
Innerchr14:59295696..59621067hg19UCSC Ensembl
Innerchr14:58365449..58690820hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38325372
hg19325372
hg18325372
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892550
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=121
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782221
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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