A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571017



Internal ID16011740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:661905..748489hg38UCSC Ensembl
Innerchr16:711905..798489hg19UCSC Ensembl
Innerchr16:651906..738490hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3886585
hg1986585
hg1886585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4825n54
Supporting Variantsnssv851743
Samples
Known GenesCCDC78, FAM173A, FBXL16, HAGHL, JMJD8, METRN, NARFL, RHBDL1, RHOT2, STUB1, WDR24, WDR90
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571017
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