A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583004



Internal ID18534599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:165476091..165528603hg38UCSC Ensembl
Innerchr2:166332601..166385113hg19UCSC Ensembl
Innerchr2:166040847..166093359hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3852513
hg1952513
hg1852513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015115
Supporting Variants
Samples
Known GenesCSRNP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3583004
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