A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3614999



Internal ID18913280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:180089087..180517083hg38UCSC Ensembl
Innerchr3:179806875..180234871hg19UCSC Ensembl
Innerchr3:181289569..181717565hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38427997
hg19427997
hg18427997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012271
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)nssv3614999
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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