A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057888



Internal ID18800419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47837173..48489530hg38UCSC Ensembl
Innerchr20:46465917..47117776hg19UCSC Ensembl
Innerchr20:45899324..46551183hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38652358
hg19651860
hg18651860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4322n100
Supporting Variantsnssv3584949
Samples
Known GenesLINC00494
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057888
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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