A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595606



Internal ID16383015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:142710538..142808442hg38UCSC Ensembl
Innerchr4:143631691..143729595hg19UCSC Ensembl
Innerchr4:143851141..143949045hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3897905
hg1997905
hg1897905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1008559
Samples
Known GenesINPP4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595606
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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