A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589489



Internal ID18887770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22603429..22687278hg38UCSC Ensembl
Innerchr3:22644920..22728769hg19UCSC Ensembl
Innerchr3:22619924..22703773hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3883850
hg1983850
hg1883850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010220
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589489
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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