A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546206



Internal ID16333615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:51989444..51990298hg38UCSC Ensembl
Innerchr1:52455116..52455970hg19UCSC Ensembl
Innerchr1:52227704..52228558hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38855
hg19855
hg18855
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv268n54
Supporting Variantsnssv712985, nssv712983, nssv712987, nssv712984, nssv712986, nssv712982
Samples
Known GenesRAB3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546206
Frequency
Sample Size17421
Observed Gain4
Observed Loss2
Observed Complex0
Frequencyn/a


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