A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571176



Internal ID16358585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1813519..1855005hg38UCSC Ensembl
Innerchr16:1863520..1905006hg19UCSC Ensembl
Innerchr16:1803521..1845007hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3841487
hg1941487
hg1841487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4857n54
Supporting Variantsnssv1148895
Samples1782681169_A
Known GenesFAHD1, HAGH, MEIOB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571176
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