A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057975



Internal ID19147194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23666845..23721368hg38UCSC Ensembl
Innerchr20:23647482..23702005hg19UCSC Ensembl
Innerchr20:23595482..23650005hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3854524
hg1954524
hg1854524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737178
Samples
Known GenesCST4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057975
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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