A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1002372



Internal ID16296328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:77370722..77413329hg38UCSC Ensembl
Innerchr4:78291876..78334483hg19UCSC Ensembl
Innerchr4:78510900..78553507hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3842608
hg1942608
hg1842608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594698
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1002372
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