A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv987694



Internal ID16281650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1493378..1521137hg38UCSC Ensembl
Innerchr4:1495105..1522864hg19UCSC Ensembl
Innerchr4:1464433..1492404hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3827760
hg1927760
hg1827972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593306
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)nssv987694
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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