A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729265



Internal ID18680860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:157303324..157624221hg38UCSC Ensembl
Innerchr2:158159836..158480733hg19UCSC Ensembl
Innerchr2:157868082..158188979hg18UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38320898
hg19320898
hg18320898
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011505
Supporting Variants
Samples
Known GenesACVR1C, CYTIP, ERMN, GALNT5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3729265
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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