A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061899



Internal ID18804430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:46498425..47439490hg38UCSC Ensembl
Innerchr20:45127064..46068234hg19UCSC Ensembl
Innerchr20:44560471..45501641hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38941066
hg19941171
hg18941171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584944
Samples
Known GenesEYA2, LOC100131496, MIR3616, OCSTAMP, SLC13A3, SLC2A10, TP53RK, ZMYND8, ZNF334
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061899
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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