A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785801



Internal ID19159847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14194215..14242305hg38UCSC Ensembl
Innerchr18:14194214..14242304hg19UCSC Ensembl
Innerchr18:14184214..14232304hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3848091
hg1948091
hg1848091
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893076
Supporting Variants
Samples
Known GenesANKRD20A5P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785801
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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