A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579544



Internal ID18531139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:95501222..95593452hg38UCSC Ensembl
Innerchr2:96166970..96259200hg19UCSC Ensembl
Innerchr2:95530697..95622927hg18UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg3892231
hg1992231
hg1892231
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008062
Supporting Variants
Samples
Known GenesTRIM43
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579544
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