A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150140



Internal ID15506824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51784199..52104512hg38UCSC Ensembl
Innerchr19:52287452..52607765hg19UCSC Ensembl
Innerchr19:56979264..57299577hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38320314
hg19320314
hg18320314
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580000
Supporting Variants
Samples1780854257_A
Known GenesFPR3, HCCAT3, ZNF350, ZNF432, ZNF577, ZNF613, ZNF614, ZNF615, ZNF649, ZNF841
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150140
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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