A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3633877



Internal ID18932158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:77599520..77632600hg38UCSC Ensembl
Innerchr4:78520674..78553754hg19UCSC Ensembl
Innerchr4:78739698..78772778hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3833081
hg1933081
hg1833081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010104
Supporting Variants
Samples
Known GenesCXCL13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3633877
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