A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782855



Internal ID19163495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:64414728..64476234hg38UCSC Ensembl
Innerchr5:63710555..63772061hg19UCSC Ensembl
Innerchr5:63746311..63807817hg18UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3861507
hg1961507
hg1861507
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894203
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782855
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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