A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1001742



Internal ID16295698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:65687707..65739511hg38UCSC Ensembl
Innerchr4:66553425..66605229hg19UCSC Ensembl
Innerchr4:66236020..66287824hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3851805
hg1951805
hg1851805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594477
Supporting Variants
Samples
Known GenesLOC100144602
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1001742
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