A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595205



Internal ID16382614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:114421377..114517952hg38UCSC Ensembl
Innerchr4:115342533..115439108hg19UCSC Ensembl
Innerchr4:115561982..115658557hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3896576
hg1996576
hg1896576
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9228n54
Supporting Variantsnssv1152826, nssv1152825
SamplesHGDP00645, HGDP00641
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595205
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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