A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv989317



Internal ID16283273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6003650..6032312hg38UCSC Ensembl
Innerchr4:6005377..6034039hg19UCSC Ensembl
Innerchr4:6056278..6084940hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3828663
hg1928663
hg1828663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593493
Supporting Variants
Samples
Known GenesJAKMIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv989317
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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