A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561496



Internal ID16348905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37496412..37544959hg38UCSC Ensembl
Innerchr13:38070549..38119096hg19UCSC Ensembl
Innerchr13:36968549..37017096hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3848548
hg1948548
hg1848548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3119n54
Supporting Variantsnssv807746, nssv807747, nssv1176441
SamplesHGDP00912
Known GenesLINC00547
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561496
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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