A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3592284



Internal ID18890565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:48675956..48702707hg38UCSC Ensembl
Innerchr22:49071768..49098519hg19UCSC Ensembl
Innerchr22:47458204..47484525hg18UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3826752
hg1926752
hg1826322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057928
Supporting Variants
Samples
Known GenesFAM19A5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3592284
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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