A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710340



Internal ID19008621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30135946..30183553hg38UCSC Ensembl
Innerchr12:30288879..30336486hg19UCSC Ensembl
Innerchr12:30180146..30227753hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3847608
hg1947608
hg1847608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035561
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710340
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