A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3641189



Internal ID18592784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:141530670..141811212hg38UCSC Ensembl
Innerchr4:142451823..142732365hg19UCSC Ensembl
Innerchr4:142671273..142951815hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38280543
hg19280543
hg18280543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018949
Supporting Variants
Samples
Known GenesIL15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3641189
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