A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592527



Internal ID16379936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173521663..173583247hg38UCSC Ensembl
Innerchr3:173239453..173301037hg19UCSC Ensembl
Innerchr3:174722147..174783731hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3861585
hg1961585
hg1861585
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8733n54
Supporting Variantsnssv981280, nssv981281, nssv981276, nssv981275, nssv981274, nssv981279, nssv981277, nssv981278
Samples
Known GenesNLGN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592527
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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