A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3617056



Internal ID18915337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..36319hg38UCSC Ensembl
Innerchr4:12269..36319hg19UCSC Ensembl
Innerchr4:2269..26319hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3824051
hg1924051
hg1824051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010960
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)nssv3617056
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