A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3469330



Internal ID18716640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16850538..16959812hg38UCSC Ensembl
Innerchr1:17177033..17286307hg19UCSC Ensembl
Innerchr1:17049620..17158894hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38109275
hg19109275
hg18109275
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002758
Supporting Variants
Samples
Known GenesCROCC, MIR3675
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3469330
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