A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593342



Internal ID16034065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1870601..1872093hg38UCSC Ensembl
Innerchr4:1872328..1873820hg19UCSC Ensembl
Innerchr4:1842126..1843618hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381493
hg191493
hg181493
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8903n54
Supporting Variantsnssv988446, nssv988448, nssv988449, nssv988447
Samples
Known GenesWHSC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593342
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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