A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3636064



Internal ID18587659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:146134466..146217245hg38UCSC Ensembl
Innerchr4:147055618..147138397hg19UCSC Ensembl
Innerchr4:147275068..147357847hg18UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3882780
hg1982780
hg1882780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018859
Supporting Variants
Samples
Known GenesLSM6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3636064
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