A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594918



Internal ID16382327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:96647091..96776919hg38UCSC Ensembl
Innerchr4:97568242..97698070hg19UCSC Ensembl
Innerchr4:97787265..97917093hg18UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38129829
hg19129829
hg18129829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1003388
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594918
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