A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593326



Internal ID16380735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1601262..1602019hg38UCSC Ensembl
Innerchr4:1602989..1603746hg19UCSC Ensembl
Innerchr4:1572949..1573706hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38758
hg19758
hg18758
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8899n54
Supporting Variantsnssv988373, nssv988412, nssv988382, nssv988368, nssv988415, nssv988408, nssv988386, nssv988403, nssv988402, nssv988396, nssv988410, nssv988394, nssv988371, nssv988418, nssv988385, nssv988387, nssv988414, nssv988384, nssv988370, nssv988392, nssv988367, nssv988419, nssv988400, nssv988411, nssv988405, nssv988407, nssv988364, nssv988395, nssv988372, nssv988420, nssv988417, nssv988404, nssv988406, nssv988398, nssv988388, nssv988409, nssv988363, nssv988397, nssv988416, nssv988381, nssv988393, nssv988389, nssv988401, nssv988391, nssv988374, nssv988379, nssv988383, nssv988375, nssv988377, nssv988378, nssv988413, nssv988369, nssv988380, nssv988399, nssv988390, nssv988376, nssv988365, nssv988366
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593326
Frequency
Sample Size17421
Observed Gain28
Observed Loss30
Observed Complex0
Frequencyn/a


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