A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592537



Internal ID16379946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173529023..173583247hg38UCSC Ensembl
Innerchr3:173246813..173301037hg19UCSC Ensembl
Innerchr3:174729507..174783731hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3854225
hg1954225
hg1854225
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8733n54
Supporting Variantsnssv1152876, nssv1152874, nssv1152875
SamplesHGDP00336, HGDP00709, HGDP00859
Known GenesNLGN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592537
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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