A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583060



Internal ID18881341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:176290690..176349860hg38UCSC Ensembl
Innerchr2:177155418..177214588hg19UCSC Ensembl
Innerchr2:176863664..176922834hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3859171
hg1959171
hg1859171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014372
Supporting Variants
Samples
Known GenesMTX2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3583060
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