A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv981629



Internal ID16275585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177576293..177579658hg38UCSC Ensembl
Innerchr3:177294081..177297446hg19UCSC Ensembl
Innerchr3:178776775..178780140hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg383366
hg193366
hg183366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592621
Supporting Variants
Samples
Known GenesLINC00578
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv981629
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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