A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571175



Internal ID16011898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1806439..1875278hg38UCSC Ensembl
Innerchr16:1856440..1925279hg19UCSC Ensembl
Innerchr16:1796441..1865280hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3868840
hg1968840
hg1868840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852072
Samples
Known GenesFAHD1, HAGH, MEIOB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571175
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