A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595604



Internal ID16383013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:142156248..142307761hg38UCSC Ensembl
Innerchr4:143077401..143228914hg19UCSC Ensembl
Innerchr4:143296851..143448364hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38151514
hg19151514
hg18151514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1008558
Samples
Known GenesINPP4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595604
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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