A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066860



Internal ID18809391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4973849..5652866hg38UCSC Ensembl
Innerchr20:4954495..5633512hg19UCSC Ensembl
Innerchr20:4902495..5581512hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38679018
hg19679018
hg18679018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3734866
Samples
Known GenesCDS2, GPCPD1, LINC00654, LINC00658, LOC643406, PCNA, PCNA-AS1, PROKR2, SLC23A2, TMEM230
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066860
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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