A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894137



Internal ID19185206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:14068322..14087524hg38UCSC Ensembl
Outerchr5:14068322..14087524hg38UCSC Ensembl
Innerchr5:14068431..14087633hg19UCSC Ensembl
Outerchr5:14068431..14087633hg19UCSC Ensembl
Innerchr5:14121431..14140633hg18UCSC Ensembl
Outerchr5:14121431..14140633hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3819203
hg1919203
hg1819203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786032
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894137
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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