A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595232



Internal ID16382641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:115007591..116586543hg38UCSC Ensembl
Innerchr4:115928747..117507699hg19UCSC Ensembl
Innerchr4:116148196..117727147hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg381578953
hg191578953
hg181578952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1005693
Samples
Known GenesMIR1973, NDST4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595232
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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