A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595952



Internal ID16036675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161406415..162238893hg38UCSC Ensembl
Innerchr4:162327567..163160045hg19UCSC Ensembl
Innerchr4:162547017..163379495hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38832479
hg19832479
hg18832479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1010297
Samples
Known GenesFSTL5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595952
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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