A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151403



Internal ID15873472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61693013..61729784hg38UCSC Ensembl
Innerchr20:60268069..60304840hg19UCSC Ensembl
Innerchr20:59701464..59738235hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3836772
hg1936772
hg1836772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586440
Supporting Variants
SamplesHGDP00208
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151403
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