A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170094



Internal ID21314155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29129882..29186909hg38UCSC Ensembl
Outerchr4:29127656..29189135hg38UCSC Ensembl
Innerchr4:29131504..29188531hg19UCSC Ensembl
Outerchr4:29129278..29190757hg19UCSC Ensembl
Innerchr4:28740602..28797629hg18UCSC Ensembl
Outerchr4:28738376..28799855hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3861480
hg1961480
hg1861480
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245198
SamplesNGO_24
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170094
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer