A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv855234



Internal ID16149190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:26901778..26943546hg38UCSC Ensembl
Innerchr16:26913099..26954867hg19UCSC Ensembl
Innerchr16:26820600..26862368hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3841769
hg1941769
hg1841769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571712
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv855234
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