A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3463746



Internal ID19060325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:38546246..38575751hg38UCSC Ensembl
Innerchr1:39011918..39041423hg19UCSC Ensembl
Innerchr1:38784505..38814010hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3829506
hg1929506
hg1829506
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997481
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)nssv3463746
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