A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893360



Internal ID19184180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63226200..63247598hg38UCSC Ensembl
Outerchr20:63226200..63247598hg38UCSC Ensembl
Innerchr20:61857552..61878950hg19UCSC Ensembl
Outerchr20:61857552..61878950hg19UCSC Ensembl
Innerchr20:61327997..61349395hg18UCSC Ensembl
Outerchr20:61327997..61349395hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3821399
hg1921399
hg1821399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781608
Samples
Known GenesBIRC7, MIR3196, NKAIN4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893360
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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