A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781648



Internal ID19160058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18636286..19057038hg38UCSC Ensembl
Innerchr13:19210426..19631178hg19UCSC Ensembl
Innerchr13:18108426..18529178hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38420753
hg19420753
hg18420753
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892294
Supporting Variants
Samples
Known GenesANKRD20A9P, LINC00408, LINC00417, LINC00442
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=68
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781648
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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