A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586616



Internal ID16027339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63736025..63738542hg38UCSC Ensembl
Innerchr20:62367377..62369895hg19UCSC Ensembl
Innerchr20:61837821..61840339hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382518
hg192519
hg182519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7677n54
Supporting Variantsnssv943844
Samples
Known GenesLIME1, ZGPAT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586616
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer