A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1019570



Internal ID16313526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186145486..186171321hg38UCSC Ensembl
Innerchr4:187066640..187092475hg19UCSC Ensembl
Innerchr4:187303634..187329469hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3825836
hg1925836
hg1825836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596400
Supporting Variants
Samples
Known GenesFAM149A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1019570
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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