A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592631



Internal ID16380040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177576993..177584329hg38UCSC Ensembl
Innerchr3:177294781..177302117hg19UCSC Ensembl
Innerchr3:178777475..178784811hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg387337
hg197337
hg187337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8752n54
Supporting Variantsnssv981768, nssv981765, nssv981766, nssv981767, nssv981769
Samples
Known GenesLINC00578
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592631
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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