A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590234



Internal ID18888515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:31065..63682hg38UCSC Ensembl
Innerchr3:72739..105365hg19UCSC Ensembl
Innerchr3:47739..80365hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3832618
hg1932627
hg1832627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012756
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)nssv3590234
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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