A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573557



Internal ID16014280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87808535..87854711hg38UCSC Ensembl
Innerchr16:87842141..87888317hg19UCSC Ensembl
Innerchr16:86399642..86445818hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3846177
hg1946177
hg1846177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv862380
Samples
Known GenesMIR6775, SLC7A5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573557
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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