A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648088



Internal ID18946369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:122897947..122926205hg38UCSC Ensembl
Innerchr5:122233642..122261900hg19UCSC Ensembl
Innerchr5:122261541..122289799hg18UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3828259
hg1928259
hg1828259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032251
Supporting Variants
Samples
Known GenesSNX24
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3648088
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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