A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153182



Internal ID15853449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152967488..152993851hg38UCSC Ensembl
Innerchr4:153888640..153915003hg19UCSC Ensembl
Innerchr4:154108090..154134453hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3826364
hg1926364
hg1826364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595745
Supporting Variants
Samples1780854205_A
Known GenesFHDC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153182
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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