A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv981611



Internal ID16275567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176141216..176189554hg38UCSC Ensembl
Innerchr3:175859004..175907342hg19UCSC Ensembl
Innerchr3:177341698..177390036hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3848339
hg1948339
hg1848339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592607
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv981611
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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