A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv979349



Internal ID15926619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163001200..163004076hg38UCSC Ensembl
Innerchr3:162718988..162721864hg19UCSC Ensembl
Innerchr3:164201682..164204558hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg382877
hg192877
hg182877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592363
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)nssv979349
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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