A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154303



Internal ID15878834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35534425..35624967hg38UCSC Ensembl
Innerchr6:35502202..35592744hg19UCSC Ensembl
Innerchr6:35610180..35700722hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3890543
hg1990543
hg1890543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602923
Supporting Variants
SamplesHGDP01266
Known GenesFKBP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154303
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