A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv981331



Internal ID16275287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:175357320..175372873hg38UCSC Ensembl
Innerchr3:175075109..175090662hg19UCSC Ensembl
Innerchr3:176557803..176573356hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3815554
hg1915554
hg1815554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592557
Supporting Variants
Samples
Known GenesMIR4789, NAALADL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv981331
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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