A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592363



Internal ID16033086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163001200..163004076hg38UCSC Ensembl
Innerchr3:162718988..162721864hg19UCSC Ensembl
Innerchr3:164201682..164204558hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg382877
hg192877
hg182877
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8701n54
Supporting Variantsnssv979353, nssv979356, nssv979345, nssv979360, nssv979359, nssv979347, nssv979349, nssv979346, nssv979354, nssv979358, nssv979355, nssv979357, nssv979352, nssv979351, nssv979350, nssv979344, nssv979348
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592363
Frequency
Sample Size17421
Observed Gain10
Observed Loss7
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer