A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852055



Internal ID15799325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1431019..1457987hg38UCSC Ensembl
Innerchr16:1481020..1507988hg19UCSC Ensembl
Innerchr16:1421021..1447989hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3826969
hg1926969
hg1826969
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571161
Supporting Variants
Samples
Known GenesCCDC154, CLCN7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852055
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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