A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1006928



Internal ID15954198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134008882..134216805hg38UCSC Ensembl
Innerchr4:134930037..135137960hg19UCSC Ensembl
Innerchr4:135149487..135357410hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38207924
hg19207924
hg18207924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595480
Supporting Variants
Samples
Known GenesPABPC4L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1006928
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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