A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786032



Internal ID19175562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:14068322..14087524hg38UCSC Ensembl
Innerchr5:14068431..14087633hg19UCSC Ensembl
Innerchr5:14121431..14140633hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3819203
hg1919203
hg1819203
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894137
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786032
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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