A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598204



Internal ID16038927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:56815393..56816476hg38UCSC Ensembl
Innerchr5:56111220..56112303hg19UCSC Ensembl
Innerchr5:56146977..56148060hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg381084
hg191084
hg181084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9790n54
Supporting Variantsnssv1030772
Samples
Known GenesMAP3K1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598204
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