A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584281



Internal ID18535876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59862589..59928674hg38UCSC Ensembl
Innerchr20:58437644..58503729hg19UCSC Ensembl
Innerchr20:57871039..57937124hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3866086
hg1966086
hg1866086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062955
Supporting Variants
Samples
Known GenesSYCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584281
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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