A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579476



Internal ID18877757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91460974..91694856hg38UCSC Ensembl
Innerchr2:91653350..91882882hg19UCSC Ensembl
Innerchr2:91017077..91246609hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38233883
hg19229533
hg18229533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011017
Supporting Variants
Samples
Known GenesLOC654342
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579476
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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