A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589952



Internal ID18888233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:81037..127687hg38UCSC Ensembl
Innerchr20:61678..108328hg19UCSC Ensembl
Innerchr20:9678..56328hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3846651
hg1946651
hg1846651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065832
Supporting Variants
Samples
Known GenesDEFB125
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589952
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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